Todos os trabalhos que foram classificados para apresentação oral, os dez trabalhos que concorrem ao prêmio de melhor poster e os 42 melhores trabalhos em poster serão publicados em edição online com acesso livre da Hormone Research in Pediatrics, um dos mais importantes periódicos científicos na área de Endocrinologia Pediátrica

Apresentação Oral

OP1 - Clinical presentation and genetic findings in the Paraganglioma Syndrome associated with mutations in SDHB (Pgl4)
Autor(es): Sanso G; Vieites A; De Miguel V; Bergada I; Barontini M;

OP2 - Predictive Cut Off Values of Basal 17-hydroxyprogesterone (17OHP) to Diagnose Non-Classic Congenital Adrenal Hyperplasia due to 21-Hydroxilase Deficiency
Autor(es): Chagas NB; Braid ZM; Coeli-Lacchini F; Castro M; Moreira AC; Mermejo LM; Antonini SR;

OP3 - SAMD9 (Sterile Alpha Motif Domain-containing 9) in Adrenocortical Tumors
Autor(es): SANTOS, C.H.; BUENO, A. C.;

OP4 - VALIDATION OF SERUM 17α-HYDROXYPROGESTERONE CONCENTRATION REFERENCE RANGES BY ELISA METHOD IN INFANTS DURING THE FIRST YEAR OF LIFE
Autor(es): Cestino ML; Breyer FA;

OP5 - INHIBITION OF IGF1R BY IGF-1R/IR INHIBITOR OSI906 AS A TARGETED THERAPY FOR GLIOBLASTOMA: IN VITRO & IN VIVO STUDIES.
Autor(es): Fernández MC; Martin A; Clément F; Venara MC; García Lombardi M; Bergadá I; Gutiérrez M; Pennisi PA;

OP6 - Bone age determination in Brazilian children and adolescents: a comparison between computerized BoneXpert, Greulich-Pyle and Tanner-Whitehouse II methods.
Autor(es): Artioli TO; Morais TK; Kochi C; Longui CA;

OP7 - Chromosomal IGF1R deletion: array characterization in two patients with structural abnormalities in chromosome 15
Autor(es): Casali B; Keselman A; Villegas F; Sanguineti, Nora; Fernandez MC; Armando R; Boywitt A; Rodolfo De Bellis; del Rey G; Arberas C; Rey R; Ropelato G; Bergadá, I;

OP8 - Clinical and genetic evaluation of prepubertal children with short stature and advanced bone age
Autor(es): Vasques GA; Andrade NLM; Funari MFA; Homma TK; Freire BL; Nishi MY; Malaquias AC; Mendonca BB; Arnhold IJP; Jorge AAL;

OP9 - Clinical aspects and common genetics polymorphisms implicated in short stature in sickle cell anemia
Autor(es): Costa-Júnior DA; Frossard TNSV; Rodrigues TMB; Santos APP; Amaral AB; Silva CM; Ferreira FO; Carvalho GQ; Madeira M; Velloso-Rodrigues C; Silva IT; Lima RLS; Cruz NRC; Neto LH;

OP10 - CONGENITAL AND ACQUIRED PITUITARY INSUFFICIENCY DURING THE TRANSITION STAGE: FIRST ARGENTINE EXPERIENCE IN THE EVALUATION OF CARDIOMETABOLIC PARAMETERS AT THE END OF GH THERAPY
Autor(es): Boquete C; Boquete HR; Sequera AM; Ruibal G; Suárez M; Azaretzky M; Fideleff G; Dzembrowski L; Nuñez Chavarria E; Fideleff HL;

OP11 - Evidence-based approach for current standardized GH, IGF-I and IGFBP-3 assays to rule out GHD in neonates and infants.
Autor(es): Braslavsky D; Keselman A; Rodriguez ME; Freire AV; Altube M; Gutierrez A; Scaglia PA; Gotta G; Ropelato MG; Bergadá I; Ballerini MG;

OP12 - Heterozygous GH1 p.R209H variant challenges the assessment of short stature
Autor(es): Braslavsky D; Sanguineti N; Scaglia P; Keselman A; Ballerini MG; Ropelato MG; Suco S; Kitzman J; Vishnopolska S; Marti M; Domené H; Rey R; Perez Millan MI; Camper SA;

OP13 - Novel familial ACAN gene mutation in a short stature family of an SGA proband
Autor(es): Kraus J; Dauber A; Hwa V; Tyzinski L; Fujimoto M;

OP14 - RESPONSE TO rhGH THERAPY IN CHILDREN WITH ISOLATED SHORT STATURE WITH OR WITHOUT AN IDENTIFIED GENETIC CAUSE
Autor(es): Andrade NLM; Vasques GA; Funari MFA; Menconca BB; Jorge AAL;

OP15 - The overweight and obesity accelerates de skeletal maturity and decrease the growth potential in Mexican children and adolescents.
Autor(es): Miranda-Lora AL; Espinosa- Espindola M; López- González D; Sánchez Curiel- Loyo Mariana; Dies-Suárez P ; Klünder- Klünder M;

OP16 - 24-hour glucose profile in healthy adults using a continuous glucose monitoring system.
Autor(es): Gaete X; CERDA T; ROMAN R.; CODNER E.;

OP17 - Acquired lipodystrophy among children and adolescents attending a diabetes camp
Autor(es): Werneck G; Dos Santos TJ; Salazar-González JJ; Pumputis FRC; Palacio J; Coll J; López M;

OP18 - BMI TRAJECTORY FROM BIRTH TO ADULTHOOD AND ITS ASSOCIATION WITH PANCREATIC β-CELL FUNCTION IN EARLY ADULTHOOD
Autor(es): BURROWS R; CORREA-BURROWS R; ROGAN J; BLANCO E; GAHAGAN S;

OP19 - CONGENITAL HYPERINSULINEMIC HYPOGLUCEMIA, OUR EXPERIENCE IN 34 PATIENTS
Autor(es): Barreto TG; Calzada R; Ruiz M; Arguinzoniz L; Altamirano N; Medina FA; Flanagan S; Aguilar L; Nishimura E;

OP20 - Development and validation of an educative manual for adolescents with type 2 diabetes.
Autor(es): Hernández Trejo KE ; Medina Bravo PG; Ibarra Delgado A; Velázquez López L; Lam Chávez AE;

OP21 - FOLLOW-UP OF PATIENTS WITH TYPE 1 DIABETES MELLITUS WHO UNDERWENT INSULIN PUMP TRAINING IN A PEDIATRIC ENDOCRINOLOGY CENTER
Autor(es): Cespedes C; Pavia MA; Forero C ; Coll M; Duran P;

OP22 - Insulin glargine 300 U/mL (Gla-300) provides effective glycemic control in youths with type 1 diabetes (T1D): the EDITION JUNIOR study
Autor(es): Danne, T; Tamborlane WT; Malievsky O; Franco D; Kawamura T; Demissie M; Niemoeller E; Goyeau H; Wardecki M; Battelino T;

OP23 - Longitudinal assessment of Klotho, FGF21, Adiponectin (Adp) and C-reactive-protein (CRP) levels in adolescents and young women with type 1 diabetes (T1D) using contraception.
Autor(es): Iñiguez G; Giraudo F; Salinas A; Merino P; Castro A; López P; Lardone MC; Cassorla F; Codner E;

OP24 - Variability in basal insulin needs in young patients with type 1 diabetes using continuous subcutaneous insulin infusion and continuous glucose monitoring with predictive low glucose insulin suspension
Autor(es): De Tezanos-Pinto A; Pichott M; Barra A; Avila A; Cassorla F; Codner E; Gaete X; Mericq V; Roman R;

OP25 - An extremely rare novel missense variant p.M304V in SOX3 gene is responsible for an X-linked GH deficiency in a Brazilian patient
Autor(es): Benedetti AFF; Silva JM; Biscotto IP; Ferreira NP; Arnhold IJP; Mendonca BB; Carvalho LRS;

OP26 - Probably Pathogenic Variants in New Candidate Genes in Patients with Pituitary Stalk Interruption Syndrome (PSIS) revealed by Whole-Exome Sequencing
Autor(es): Correa FA; Nakaguma M; Jorge AAL; Funari MFA; Lerario AM; Carvalho LRS; Arnhold IJP; Mendonca BB;

OP27 - Use of Desmopressin for Bilateral Inferior Petrosal Sinus Sampling (BIPSS) in Pediatric Patients with Cushing Disease (CD).
Autor(es): Di Palma MI; Plomer P; Gil S; Vaiani E; Viterbo G; Requejo F; Gonzalez Ramos J; Lazzati JM; Lubieniecki F; Rugilo C; Ciaccio M;

OP28 - Etiologies and clinical presentation of persistent hypoparathyroidism (HPT) in 61 children in a single tertiary center
Autor(es): Soto MF; Aziz M; Herzovich V; Dujovne N; Gazek N; Gutièrrez G; Ramirez P; Oleastro M; Obregon MG; Ayarzabal V; Ciaccio M; Gil S; Viterbo G;

OP29 - Hypercalcemia secondary to disseminated BCGitis in a boy with Mendelian Susceptibility to Mycobacteria (MSMD) due to mutation in IFN-ɣ receptor 1 gene (IFNGR1)
Autor(es): Soto MF; Mattone MC; Morales CA; Oleastro M; Palma A; Urdinez L; Viterbo GL;

OP30 - Neonatal multiple bone fractures and respiratory distress secondary to congenital hyperparathyroidism
Autor(es): Plomer PG; Soto MF; De Dona V; Dujovne N; Gil S; Vaiani E; Viterbo G;

OP31 - Osteogenesis imperfecta type I: which patients should be treated with aminobisphosphonates?
Autor(es): Santos IN; Menezes Filho HC ; Franco, RR; Cominato L; Steinmetz L; Manna TD; Damiani D;

OP32 - Use of anti-FGF23 monoclonal antibody in the treatment of children and adolescents with X-Linked Hypophosphatemic Rickets.
Autor(es): Hamilton; L Brenzoni; V Forclaz; S D´Amato; Rosenfeld P; Bergada I; Alconcher L;

OP33 - BMI throughout the life-course and its relation with cardiometabolic disorders in early adulthood: results from the Santiago Longitudinal Study
Autor(es): BURROWS R; CORREA-BURROWS P; ROGAN J; BLANCO E; GAHAGAN S;

OP34 - Changes on Gut Microbiota After Laparoscopic Sleeve Gastrectomy in Adolescence: Case Reports.
Autor(es): Rachid L; Cominato L; Franco RR; Cortez RV; Moreira LN; Frascino A; Taddei CR; Steinmetz L; Della Manna T; Velhote MCP; Filho HCM; Toma RK; Damiani D;

OP35 - Differences between short- and long-term outcomes of laparoscopic sleeve gastrectomy in adolescence.
Autor(es): Franco RR; Cominato L; Ybarra M; Rachid L; Jeronimo T; Potter M; Steinmetz L; Manna TD; Menezes Filho HC; velhote MC; Durval D;

OP36 - Nonalcoholic Fatty Liver Disease and morbid obese adolescent submitted to a bariatric surgery.
Autor(es): Cominato L; Franco RR; rachid l; Frascino A; Leandra Steinmetz; Manna TD; Velhote MC; Menezes Filho HC; ybarra m; Deboni M; Toma RK; Porta G; Damiani D;

OP37 - 47,XXY/46,XX chromosomal DSD: challenges in the diagnosis and management
Autor(es): Bastida MG; Grinspon R; Avila S; De Carli C; Diaz S; Venara M; Bergada I; Rey MR;

OP38 - A Novel Anti-Müllerian Hormone (AMH) Gene Mutation in a Patient with Persistent Müllerian Duct Syndrome (PMDS) type 1
Autor(es): Mattone MC; Lobo de la Vega V; D’Alessandro P; Marino R; Perez Garrido N; Galluzzo ML; Costanzo M; Zaidman V; Lazzati JM; Berensztein E; Ramirez P; Touzon MS; Ciaccio M; Belgorosky A; Bailez M; Guercio G;

OP39 - Characteristics of transgender children and adolescent patients in a pediatric hospital: Multidisciplinary approach
Autor(es): Figueroa Gacitúa V; Sanz C; Nigro N; Lopez Dacal J; Gallardo R; Brunetto O H;

OP40 - DHX37: a new player in 46,XY gonadal dysgenesis
Autor(es): Costanzo M; Guercio G; Touzon MS; Marino R; Mattone C; Ramirez P; Perez Garrido N; Lazzati JM; Zaidman V; Galluzo L; Bailez M; Berensztein E; Ciaccio M; Belgorosky A;

OP41 - DSD, BONE DYSPLASIA, AND THE Y CHROMOSOME?
Autor(es): Mendoza Rojas VC; Contreras García GA;

OP42 - Evaluation of puberty in patients with Noonan syndrome and mutations in the RAS/MAPK genes.
Autor(es): Malaquias AC; Noronha RM; Homma TK; Albuquerque EVA; Vasques GA; Bertola DR; Jorge AAL;

OP43 - Puberty and Growth in Boys with Constitutional Delay of Growth and Puberty
Autor(es): Luciano TM; Stecchini MF; de Almeida LEA; Bettiol H; Cardoso VC; Aragon DC; Antonini SR;

OP44 - Safety of chemotherapy for hematologic malignancies as regards testicular endocrine function in children and teenagers
Autor(es): Romina P. Grinspon; María Arozarena; Silvina Prada; Graciela Bargman; María Sanzone; Marjorie Morales Bazurto; Marcela Gutiérrez; Patricia Bedecarrás; Ana Kannemann; Graciela O. Elena ; Silvia Gottlieb; Ariel J. Berenstein; María Gabriela Ropelato; Ignacio Bergadá; Luis A. Aversa; Rodolfo A. Rey;

OP45 - EVALUATION OF PUBLIC CONGENITAL HYPOTHYROIDISM SCREENING PROGRAM IN SOUTHERN BRAZIL AFTER TSH CUTOFF REDUCTION
Autor(es): Rizzotto MIB; Carreiro S; Garcia RMR; Selistre L; Vargas PR; Mastella L; Castro SM; Kopacek C;

OP46 - Factors associated with neonatal hyperthyroidism in neonates born to mothers with Graves‘ disease
Autor(es): Munoz T; Roman R;

OP47 - Male individuals with Autoimmune Thyroid Disease present higher risk for clustering other Non-Thyroidal Autoimmune Diseases
Autor(es): Lopes FSC; Almeida MAAL; Pratesi R; Oliveira RS; Castro LC;

OP48 - The usefulness of free T3 and free T3/free T4 ratio in the differential diagnosis between non-thyroidal illness and central hypothyroidism in pediatric children
Autor(es): Garín Gómez S; Zaidman V; Herzovich V; Dujovne N; Gazek N; Florio S; Belgorosky A; Ciaccio M; Lazzati JM;



Apresentação Pôster

Adrenal

PP1 - Childhood adrenocortical carcinoma: Case report
Autor(es): Ana Rocha R.; Carolina Sepulveda R.; Andrea Perez; Vivian Gallardo; Soledad VillanuevaT.; Anahi Yizmeyian;

PP2 - Clinical and biochemical features at the diagnosis of a large cohort of patients diagnosed with the classic form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Autor(es): Braid, Zilda; CASTRO, M; MERMEJO, LÍVIA M.; ANTONINI, S R.; MOREIRA, A. C;

PP3 - Congenital Adrenal Hyperplasia (CAH): Case report of a compound heterozygote CYP21A2 mutation with high glucocorticoids (GC) sensibility
Autor(es): Obeid BL; Castro ABS; Franco RR; Cominato L; Steinmetz L; Manna TD; Filho HCM; Semer B; Carvalho DF; Bachega T; Damiani D;

PP4 - CONGENITAL ADRENAL HYPERPLASIA: Clinical and molecular profile of newborns detected after 5 years of public screening program implementation
Autor(es): Kopacek C; Beltrão LA; Wiest P; Vargas PR; Krebs I; Castro SM;

PP5 - Differential Diagnosis of Virilization in Prepubertal Children: Case Report
Autor(es): Bordin L; Bitencourt BB; Ferreira R; Oliveira LS; França FV; Hasselmann PF; Kraemer GC; França SN; Pereira RM;

PP6 - Early diagnosis of adrenocortical carcinoma due to elevated 17-hydroxyprogesterone in newborn screening.
Autor(es): Garcia TS; Erbes JM; Lee JS; Cechinel E; Simoni G; Nascimento ML ; Silva PCA;

PP7 - Experience in a Screening program for Congenital Adrenal Hyperplasia between 2010-2018
Autor(es): Vitale LE; Gonzalez V; Morín A; Tournier A; Borrajo G; Marino R; Belgorosky A; Santucci Z; Balbi V; Fasano MV;

PP8 - IN2 AND V281L MUTATION OF THE CYP21A2 GEN AS A CAUSE OF SUPRARENAL HYPERPLASIA
Autor(es): Mejia de Beldjenna L; Contreras D; Perez MC ; Rios C;

PP9 - Initial assessment of patients with high levels of 17-alpha-hydroxyprogesterone (17-OHP) at neonatal screening (NS): Clinical and laboratorial profile
Autor(es): Diniz ALO; Costa MW; Cabral Menezes-Filho H; Franco, RR; Steinmetz L; Cominato L; Della Manna T; Damiani D;

PP10 - Prevalence of polymorphisms of the NR3C1 gene related to glucocorticoid sensitivity in patients with congenital adrenal hyperplasia
Autor(es): Soares NF; Villela TR; Barra CB; Silva ACS; Belisário AR; Silva IN;

PP11 - Revisiting incidence of congenital adrenal hyperplasia in the State of Minas Gerais - Brazil
Autor(es): Soares NF; Ferreira TL; Mafra JR; Oliveira LE; Silva LCB; Barra CB; Mantovani RM; Pezzuti IL; Silva IN;

PP12 - Slow progression of a large adrenocortical carcinoma in a pediatric patient
Autor(es): Lopez Dacal J; Gallardo R; Cassanova A; Basile C; Denes E; Navacchia D; Brunetto O; Figueroa Gacitua V;

PP13 - UNCOMMON FINDINGS IN BECKWITH-WIEDEMANN SYNDROME
Autor(es): ERBES JM; GARCIA TS; LEE JS; CECHINEL E; SIMONI G; NASCIMENTO ML; SILVA PCA;

PP14 - VIRILIZATION IN AN ADOLESCENT GIRL: OVARIAN HYPERTHECOSIS?
Autor(es): Oliveira LS; França FV; Hasselmann PF; Bordin L; Kraemer GC; Carvalho JAR; Pereira RM; Franla SN; Demartini AC; Lacerda Filho L;


Crescimento

PP15 - A girl with short stature
Autor(es): Morales, CA; Costanzo M; Ciaccio M; Di Palma MI;

PP16 - Adherence and long-term outcomes of therapy in pediatric subjects in Argentina using easypod™ electromechanical device for growth hormone treatment: the Phase IV multicentre Easypod™ Connect Observational Study (ECOS)
Autor(es): C.Chareca; A.Belgorosky; J.Chiarpenello; L.Colombi; T. Pasqualini; C.Von Schulz Hausmann; A.Assefi; M.Miras;

PP17 - ANALYSIS OF SURVEY CARRIED OUT TO CHILEAN PROFESSIONALS ON THE PERCEPTION OF ADHERENCE OF PEDIATRIC PATIENTS TREATED WITH GROWTH HORMONE
Autor(es): De Tezanos-Pinto A; Hernandez MI;

PP19 - Excellent response to Growth Hormone and GnRH analogue treatment in a patient with Floating Harbor Syndrome
Autor(es): Aziz M; Plomer PG; Obregon MG; Ciaccio M;

PP20 - Growth and clinical characteristics of children with Floating-Harbor syndrome: analysis of current original data and a review of the literature
Autor(es): Malaquias AC; Homma TK; Freire BL; Honjo R; Dauber A; Funari MFA; Lerario AM; Albuquerque EV; Vasques GA; Bertola DR; Kim CA; Jorge AAL;

PP21 - Growth hormone (GH) therapy in disproportionate short children with skeletal dysplasias
Autor(es): Arruda BF; Malaquias, AC; Cabral, MM; Padua, JR; Gurjao, MM;

PP22 - Growth hormone treatment adherence in patients from an emerging economy country: 1-year real-world data from the easypod™ connect eHealth platform
Autor(es): Calliari, LEP; Barquero, P; Sato, C;

PP23 - Growth response and pubertal development in children with Growth Hormone deficiency and spontaneous puberty
Autor(es): Reinoso AS; Ricci J; Martín R; Fasano MV; Morín A; Balbi VA;

PP24 - Positive impact on adherence through educational activities of the Argentina´s Patient Support Program in children with low adherence to treatment with recombinant Growth Hormone (easypod applicator).
Autor(es): A.Assefi; C.Chareca; F.Roca; P.Celis Ayala; A.Rubstein; C.Von Schulz Hausmann;

PP25 - PROFILE OF PATIENTS TREATED WITH RECOMBINANT GROWTH HORMONE IN A REFERRAL CENTER
Autor(es): Batschauer A; Baroncini CV; Lacerda Filho L; França SN; Pereira RM; Demartini AC; Kraemer GC; Cat MNL; Carvalho JAR;

PP26 - Treatment With Growth Hormone in Mexican Girls With Turner Syndrome.
Autor(es): POSADAS MENDOZA KJ; Bonilla Medina PS ; Ruiz Reyes ML ; Calzada-León R; Arguinzoniz-Valenzuela SL ; Robles Valdés C;

PP27 - Validation of the parenteral presentation of clonidine for oral use in growth hormone provocative test
Autor(es): Fittipaldi Y.; Troiano M.; Kuspiel MF; Pasqualini T.; Alonso G.;


Diabetes e Hipoglicemia

PP28 - Acute Disseminated Encephalomyelitis (ADEM) preceding Type 1 Diabetes: What is the role of anti-GAD?
Autor(es): Rossi ICB; Fernandes RGAL; Carvalho LC; Gomes DC;

PP29 - Association between hyperinsulinemia and Helicobacter pylori infection
Autor(es): Hayes Dorado JP; Rossell Lopez MA; Vaca Torruella M; Frias Eid OD; Urizar Parada V;

PP30 - Association between IGF-1 and non-alcoholic fatty liver disease in adolescents with type 2 diabetes mellitus
Autor(es): Martínez LG; Orozco JA; Medina PG;

PP31 - Changing the management of neonatal diabetes by means of genetic studies
Autor(es): Mejia L; Acevedo G; Astudillo E; Corredor V;

PP32 - Chronic mucocutaneous candidiasis and type 1 Diabetes in a child with STAT1 gain of function heterozygous mutation.
Autor(es): Pires JVG; Rodrigues R; Segundo GR; Gomes DC;

PP33 - Clinical and laboratory characteristics in Mexican adolescents with newly diagnosed Type 2 Diabetes.
Autor(es): Barrientos-Perez M; Gonzalez-Moreno Rosalba; Vázquez-Barrientos JC;

PP34 - Clinical, laboratory and glycemic variability profile in a group of T1DM patients attended at a Public University Hospital in the southeast Brazil
Autor(es): Rossi ICB; Rossi BF; Gomes DC; Rodrigues R;

PP35 - Congenital Hyperinsulinism: casuistry report in 10 years of work.
Autor(es): Insúa Beverina MA; Pacheco MGL; Filtrin MR; Tangari A;

PP36 - ENDOTHELIAL DYSFUNCTION AND ATHEROGENIC RISK FACTORS IN ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS.
Autor(es): Valdés W; Espinosa TM; Cabrera JO; Domínguez E;

PP37 - Evaluation of self-care of pediatric diabetic patients followed in an educational program of type 1 diabetes mellitus
Autor(es): Piana MP; Mantovani RM; Villela TR; Canton JMS; Silva IN;

PP38 - Growth assessment in type 1 diabetes mellitus patients attended at the Pediatric Endocrinology Outpatient Clinic of a Federal District Regional Hospital, between 2015 and 2017.
Autor(es): PACHECO NSS; SILVA JM; ALEXANDRE AR; NOGUEIRA JR; BOTELHO NRL; GATTO LRS; RODRIGUES TB; MATSUURA CO; FALLEIROS RKMM; AMORIM BRV; SOUZA JL; TURRA CTD;

PP39 - HNF4A variant causing Congenital Hyperinsulinism: A case report
Autor(es): Gariza AC; La Serna JE;

PP40 - Hyperinsulinemic Hypoglycemia Secondary to Insulinoma in Teenage: Case Report
Autor(es): Schuler TA; Araújo JR; Gomes BGS; Ferreira AHA; Souza KP; Alves KTS; Fernandes ALPR; Gonzalez MMP; Lauro GP; Pereira GCL; Nascimento WE; Andrade MMD;

PP41 - NEONATAL DIABETES MELLITUS RESPONSIVE TO SULPHONYLUREA, DUE TO KCNJ11 MUTATION
Autor(es): ERBES JM; GARCIA TS; LEE JS; CECHINEL E; SIMONI G; NASCIMENTO ML; SILVA PCA;

PP42 - Post-Transplant Diabetes Mellitus in twins with autosomal dominant polycystic kidney disease: A case report
Autor(es): Silva Camarena M.; Calzada León R.; Altamirano Bustamante N.; Arguinzoniz Valenzuela L.; Ruiz Reyes M.; Robles Valdés R.;

PP43 - TYPE 2 DIABETES IN CHILDREN AND ADOLESCENTS: IS IT A REALITY IN SOUTH BRAZIL?
Autor(es): Godinho AM; Dall´Agnese A; Fornari A; Lavigne S; Vissoky GC; Geremia C; Bressiani M; Tschiedel B; Puñales M;

PP45 - Wolfram Syndrome: a cause of monogenic diabetes
Autor(es): ERBES JM; GARCIA TS; LEE JS; CECHINEL E; SIMONI G; NASCIMENTO ML; SILVA PCA;


Genética

PP47 - Berardinelli Seip Syndrome: Case report
Autor(es): Bergol MFR; Ferragini AA; Cassânego CP; Lima MK; Romão A; Cristovam MAS; Sandrini F;

PP48 - CHARACTERIZATION OF PATIENTS WITH SYNDROME OF MC CUNE ALBRIGHT AND ITS MUTATION OF THE GNSI GENE
Autor(es): Mejia de beldjenna L; Apraez K; Alvarez T; Lammoglia JJ;

PP49 - Familial hypercholesterolemia: a case report
Autor(es): Sales, MTA; Linhares, NPD; Pereira, RABO; Cavalcante, ALVM; Martins, LV; Gonçalves, CS; Sousa, MS; Aragão, LFF; Carvalho, AB; Montenegro, APDR; Gurgel, MHC;

PP50 - Giant cell tumor in a patient with Noonan syndrome
Autor(es): Paulina Schneider; Javiera Basaure; Guillermo Lay-Son; Verónica Palacios; Hugo Cooper;

PP51 - Low frequency of pathogenic allelic variants in the 46,XY differences of sex development (DSD)-related genes in small for gestational age children with hypospadias
Autor(es): Braga BL; Gomes LN; Nishi MY; Freire BL; Batista RL; Funari MFA; Costa EMF; Lerario AM; Domenice S; Junior JADF; Jorge AAL; Mendonca BB;

PP52 - Multiple Hamartoma Syndrome.Presentation of a case from multinodular goiter
Autor(es): Villanueva S; Gárate I; Gallardo V; Yizmeyian A; Rocha A; Sepúlveda C;

PP53 - Novel mutations in the AVP-NPII gene associated with neurohypophyseal diabetes insipidus
Autor(es): Garcia-Castaño A; Madariaga L; Pérez de Nanclares G; Vela A; Rica I; Gaztambide S; Martínez R; Martínez de LaPiscina I; Urrutia I; Aguayo A; Velasco O; Familial neurohypophyseal diabetes insipidus Spanish working group; Castaño L;

PP54 - Screening of c-KIT genetic variants in patients with isolated bilateral cryptorchidism
Autor(es): Rodríguez F; Herrera I; Pieper D; Cassorla F;

PP55 - Variants of Uncertain Significance (“VUS”) in 2 patients with a RASopathie phenotype (Noonan Syndrome)
Autor(es): Arriaza Z. MI; González G. Marcela; Zepeda D.; Rodriguez F;


Hipófise/Hipotálamo

PP57 - Classical phenylketonuria about a case
Autor(es): Colmenarez JL; Faria DJ;

PP58 - McCune-Albright Syndrome (MAS) associated with Cushing Syndrome (CS) in a 3-months old infant girl: preliminary results of ketoconazole treatment.
Autor(es): Ferreira R; Lacerda Filho L; Pereira RM; França SN; Demartini AC; Kraemer GC; Carvalho JAR; Bordin L;

PP59 - Metacromatic Leukodistrophy and Central Hypothyroidism, regarding a case
Autor(es): Ramos K;

PP60 - NEAR ADULT HEIGHT ACCORDING TO GENETIC TARGET IN A GIRL WITH MCCUNE ALBRIGHT SYNDROME AND GROWTH HORMONE EXCESS: 12.86 YEARS FOLLOW-UP.
Autor(es): Fernández Mentaberry M V; Riu C.; Oneto A.; Stivel M.;

PP61 - The severity of GH deficiency (GHD) does not affect adherence to treatment in GHD prepubertal children taking rGH via the Easypod device
Autor(es): Loche S;

PP62 - WHEN HAVING TOO MUCH HEIGHT IS A PROBLEM ... A CASE REPORT
Autor(es): López Avellaneda C; Guntsche Z.; Breyer F; Pott Godoy C.; Recabarren A.; Marquez P.; Cuglia N;


Metabolismo osteomineral e vitamina D

PP63 - ADEQUACY OF IRON AND VITAMIN D SUPPLEMENTATION OF CHILDREN BETWEEN ZERO AND TWO YEARS OLD ATTENDED IN A PEDIATRIC AMBULATORY
Autor(es): Vescovi JS; Vescovi ES; Mazzucchetti L; Remor KVT;

PP64 - ATYPICAL PRESENTATION OF VITAMIN D DEPENDENT RICKETS TYPE 1A (VDDR 1A)
Autor(es): Malosetti MC ; Garciarena MA; Vaiani E; Perez Garrido N; Marino R; Belgorosky A;

PP65 - Body mass index presents a strong correlation with Dual X-Ray Absorptiometry-measured adiposity in pediatric patients with Osteogenesis Imperfecta
Autor(es): Pacheco NS; Carlos GA; Chianca LS; Alexandre AR; Silva JM; Oliveira RS; Lopes FSC; Castro LC;

PP66 - Bone evaluation of children and adolescents with Turner Syndrome by quantitative ultrasound of proximal phalanges (QUS)
Autor(es): SALAZAR, KAA; FILGUEIRAS, MFTF; MENDES, LL; CUNHA, SB;

PP67 - Brucks Syndrome, a rare form of Osteogenesis Imperfecta
Autor(es): Garcia TS; Erbes JM; Lee JS; Cechinel E; Simoni G; Nascimento ML ; Silva PCA ;

PP68 - Evaluation of the osteometabolic profile of subjects in the transition phase who were treated with human recombinant growth hormone in childhood. 
Autor(es): Castro ABS; Leone C; Carneiro MS; Damiani D; Kuba VM;

PP69 - Follow up of surgical parathyroidectomy in chronic renal failure patients
Autor(es): Kuspiel Maria Florencia; Troiano Marina; Pasqualini Titania; Alonso Guillermo;

PP70 - Four novel PHEX gene mutations in patients with X-Linked Hypophosphatemia
Autor(es): Silva JM; Alexandre AR; Matsuura CO; Rodrigues TB; Pacheco NSS; Oliveira RS; Lopes FSC; Castro LC;

PP71 - Hypophosphatemic rickets: case report on the diagnosis of rare and variable disease in a family
Autor(es): Jacob CGF; Coelho AP; Villar HCCE; Toreto TMR; Silva LFHF; Ramos LP; Casagrande WM; Borges MM; Amico MMD; Buzzetto AR; Ariosa GZDA;

PP73 - Impact of phosphate and calcitriol supplementation on height and skeletal deformities of patients with X-Linked Hypophosphatemia
Autor(es): Matsuura CO; Rodrigues TB; Pacheco NSS; Alexandre AR; Silva JM; Lopes FSC; Oliveira RS; Castro LC;

PP74 - No difference in the proportion of overweight and obesity among pediatric patients with Osteogenesis Imperfecta throughout a ten-year period
Autor(es): Rodrigues TB; Chianca LS; Carlos GA; Matsuura CO; Silva JM; Alexandre AR; Lopes FSC; Oliveira RS; Castro LC;

PP75 - Parathyroid Adenomas in Pediatrics
Autor(es): Mejia de Beldjenna L; Rodriguez MI; Gomez JF;

PP76 - PHENOTYPE AND GENOTHYPE OF X-LINKED HYPOPHOSPHATEMIC RICKETS IN EIGHT BRAZILIAN CHILDREN AND ADOLESCENTS
Autor(es): Bitencourt BB; Lacerda Filho L ; França SN; Pereira RM; Demartini AC; Kraemer GC; Silvestre L; Carvalho JAR;


Neoplasia

PP77 - Atypical presentation of prolactinoma in childhood.
Autor(es): Fernandes RGAL; Rossi ISB; Feibelmann TCM; Silva ACAL; Castro SC; Lamberti MO; Gomes DC;

PP78 - Endocrinological effects of cancer and its treatment in childhood
Autor(es): Galvão BS; Rezende LM; Machado LD; Ferreira M; Esteves TC;

PP79 - LONG-TERM EVALUATION OF OVARIAN FUNCTION AND FOLLICULAR RESERVE IN PATIENTS WITH MALIGNANT DISEASES TREATED WITH CHEMOTHERAPY IN PREPUBERTAL OR PUBERTAL AGE
Autor(es): Arcari AJ; Freire AV; Grinspon RP; Bedecarrás P; Escobar ME; Ropelato MG; Bergadá IB; Rey RA; Gryngarten MG;

PP80 - Men 1 presentation with insulinoma before 10 years old: case report
Autor(es): Minaberry L; Viale ML; García Minuzzi M; Figueroa Gacitúa V;

PP81 - Peripheral precocious puberty secondary to sexual cord ovarian tumor with annular tubules (TCSTAs) not associated with Peutz-Jeghers syndrome (SPJ)
Autor(es): Garciarena MA ; Rubaja MS ; Vaiani E; Gattari P; Di Matteo E; De La Pía J; Alvarez M; Malosetti MC ;


Obesidade

PP82 - Evaluation of Inflammatory Markers, Metabolic Syndrome, hepatic steatosis and measurement of carotid intima in obese juvenile patients
Autor(es): Fernandez Alonso A; Bichara L; Chahla R; Chaila Z; Dupuy M; Elias A; Gines S; Granito S; Graif O; Guerrero C; Simesen G; Bazan C;

PP83 - Evaluation of visceral fat by ultrasound in children and adolescents
Autor(es): Piovezan JM; Alvarenga M Q; Rezende LM; Machado LD; Machado IM; Ferreira M; Carmo WB;

PP84 - Hypovitaminosis D in a group of children with obesity and risk of metabolic syndrome.
Autor(es): Menezes CA; Queiroz AS; Vasconcelos RS;

PP85 - IMPACT OF PROBIOTIC THERAPY INTERVENTION ON THE ANTHROPOMETRY OF OBESE CHILDREN AND ADOLESCENTS
Autor(es): Pellicciari CR; Pacheco TL; Artioli TO; Leiderman, DBD; Mimica, MJ; Longui CA; Kochi C;

PP86 - LEVELS OF VITAMIN D AND ITS ASSOCIATION WITH EARLY MARKERS OF CARDIOVASCULAR DISEASE IN CHILDREN AND ADOLESCENTS WITH OVERWEIGHT OR OBESITY
Autor(es): Rodriguez Azrak MS; Klajn DS; Brich TAM; Pipman VR;

PP87 - NUTRITIONAL STATE OF ADOLESCENTS IN THE STATE OF GOIÁS, BRAZIL, IN 2008 AND 2018.
Autor(es): Silva JVP; Nascimento Jr OL; Silva RDCH; Souza CSB; Oliveira LCV; Pinto RM;

PP88 - NUTRITIONAL STATE OF INFANTS UNDER 6 MONTHS OF AGE IN THE STATE OF GOIÁS, BRAZIL, IN 2008 AND 2018
Autor(es): Monteiro GMC; Cavallini LF; Nascimento Jr OL; Oliveira MA; Souza CSB; Pinto RM;

PP89 - NUTRITIONAL STATE OF PRESCHOOL CHILDREN IN THE STATE OF GOIÁS, BRAZIL, IN 2008 AND 2018
Autor(es): Resende RC; Nascimento Jr OL; Oliveira ALV; Freitas PHR; Santos HV; Souza CSB; Pinto RM;

PP90 - Obesity and cardiovascular risk factors in overweight children after at least one year of nutritional intervention
Autor(es): Barreto MCA; Solberg PFC; Gilban DLS; Bordallo AP; Gazolla FM; Assumpção COA; Luz CC; Rodrigues NCP; Oliveira CL; Madeira IR;

PP91 - Prader-Willi Syndrome and Type 2 Diabetes Mellitus
Autor(es): linhares, NPD; Pereira, RABO; Sales, MTAS; Cavalcante, ALVM; Gonçalves, CS; Montenegro, APDR; Carvalho, AB; Sousa, MS; Aragão, LFF;

PP92 - ROHHAD, a rare and challenging syndrome
Autor(es): Garcia TS; Campos Neto MB ; Erbes JM; Lee JS; Cechinel E; Simoni G; Nascimento ML ; Silva PCA;


Outros

PP93 - Association between dyslipidemia and Helicobacter pylori infection
Autor(es): Hayes Dorado JP; Eid Lit M; Gorena Montalvo CC; Barbehito Espinoza BK; Herran Cespedes Y;

PP94 - HEMATOCRIT CORRECTION: AN INNOVATIVE TOOL TO REDUCE THE RECALL RATE IN NEWBORN SCREENING OF ENDOCRINOPHATIES
Autor(es): Vilche Juarez A.; Dratler G.; Marino S.; Tommasi F.; Quiroga S.; Coniglio S.; Ciaccio M.;


Puberdade e DDS

PP95 - 5 ALPHA REDUCTASE DEFICIENCY A FAMILY REPORT
Autor(es): POSADAS MENDOZA KJ; BONILLA MEDINA PS; RUIZ REYES ML; CALZADA LEON R; Arguinzoniz Valenzuela L; Bustamante NF ; Robles Valdés C ; Yokoyama Rebollar E; Tapia Hernández B;

PP96 - Anti-Müllerian hormone reference values in paediatric population by electroquimioluminiscence
Autor(es): Ochetti M; Silvano L; Campi V; Sobrero G; Tarifa C; Martin S; Signorino M; Boyanovsky L; Pelliza C; Castro L; Muñoz L; Miras M;

PP97 - Determining factors in the continuity of care in patients with Turner Syndrome during transition.
Autor(es): Alonso G; Troiano M; Fittipaldi Y; Kuspiel MF; Paissan A; Pasqualini T;

PP98 - Development of a LC-MS/MS method to measure simultaneously 10 sexual steroids in Pediatric Endocrinology.
Autor(es): Ambao V; Rodríguez ME; Altube M; Ballerini MG; Bergadá I; Rey RA; Ropelato MG;

PP99 - Diagnostic Challenges in Sex Development Disorders: a Case Report
Autor(es): Klink GA; Lima DM; Steinmetz L; Cominato L; Franco RR; Menezes Filho HC; Della Manna T; Cespedes WCJ; Semer B; Damiani D;

PP100 - Disorders of sexual differentiation experience in the last five years in Mexican children.
Autor(es): Bonilla PS; Posadas KS; Ruiz MDLL; Sletza AV; Calzada R; Altamirano Nelly; Robles C;

PP101 - Evolution of BMI in girls under GnRHa treatment for Idiopathic Central Precocious Puberty.
Autor(es): Rampi MG; Cecchi G; Della Pia B; Fontana ML; Forrester A;

PP102 - Final height evaluation in girls with constitutional early puberty in clinical follow-up.
Autor(es): Jaconis SB; Amendola RM; D‘Souza-Li LFR;

PP103 - Genital abnormalities and pubertal development in a cohort of Prader Willi Syndrome patients
Autor(es): Berbara, HMBL; Beserra, ICR;

PP104 - GnRH analogues treatment: evolution of BMI and body adiposity index
Autor(es): Silva Camarena M.; Calzada León R.; Altamirano Bustamante N.; Arguinzoniz Valenzuela L.; Ruiz Reyes M.; Robles Valdés R.; Orellana Cardenas P.; Vargas Vázquez T.; Silva Camarena MA.;

PP105 - Is ovarian hyperstimulation syndrome in preterm infants a rare entity? Nine patients in four years from one single centre.
Autor(es): Fernandez Mentaberry M V; Bertani G; Riu C; Boichetta G; Otero P; Peisajovich I; Minotti F.; Stivel M;

PP106 - MCCUNE - ALBRIGHT SYNDROME: PHENOTYPE OF PATIENTS TREATED AT A REFERRAL CENTER AND RESPONSE TO KETOCONAZOLE TREATMENT
Autor(es): Ferreira R; Lacerda Filho L; França SN; Pereira RM; Demartini AC; Kraemer GC; Bordin L; Carvalho JAR;

PP107 - OVOTESTICULAR SEXUAL DIFFERENTIATION DISORDER. EXPERIENCE OF THE FEDERICO GÓMEZ CHILDREN‘S HOSPITAL OF MEXICO
Autor(es): Hernández Trejo KE; Martínez Domínguez LG; Baltodano Martínez YV; Elisa Cerón C; Molina Díaz M; Morales Camacho WJ;

PP108 - Partial androgen insensitivity syndrome and phenotypic variation with the same molecular mutation
Autor(es): Gallardo R; Lopez Dacal J; Marino R; Orellano M; Brunetto O; Figueroa Gacitúa V;

PP109 - PERIPHERAL PRECOCIOUS PUBERTY IN A GIRL SECONDARY TO SEX CORD TUMOR WITH ANNULAR TUBULES
Autor(es): Villatoro G; Espinoza LM; Nuñez EA;

PP110 - Precocious central puberty due to an ependymoma, regarding a case
Autor(es): Karen Ramos Rodríguez;

PP111 - Puberty in patients with Ovotesticular DSD: evaluation of 20 patients
Autor(es): Melardi JW; Cunha DFS; Cespedes WCJ; Carvalho FM; Cominato L; Menezes Filho HC; Manna TD; Franco RR; Semer B; Steinmetz L; Damiani D;

PP112 - RARE VARIANTS of TURNER SYNDROME: clinical presentation and cytogenetics in two cases.
Autor(es): Insúa Beverina MA; Arias Cau AC; Huidobro Ruiz P; Martinez Taibo C; Salim E; Hernandez SC; Nader JF;

PP113 - Sexual mosaisisms. Case report
Autor(es): Espinosa RT; Valdés GW; López PH; Leyva GG;

PP114 - Testicular Macrophage Subpopulations in Androgen Insensitivity Syndrome
Autor(es): Berensztein E; Rivarola MA ; Belgorosky A;

PP115 - Vaginal Endodermal Sinus Tumor (Yolk Sac Tumor) And Premature Thelarche Simulating A Precocious Puberty: A Case Report
Autor(es): Novaes ACL; Miranda Neto LFR; Rocha IN; Parente IX; Carvalho CAS; Rosales FHD; Ribeiro IM; Costa AN; Silva GTO;


Tireoide

PP116 - A novel mutation in the thyroid hormone receptor β gene in a patient who developed thyroid nodules
Autor(es): Hidalgo Coronado L; Chamoux A; Brunetto O; Bre M; Laham M; Adrover E; Molina M; Rivolta CM;

PP117 - Antithyroid drug treatment in children and teenagers with Graves’ disease
Autor(es): Vasconcellos GL; Beserra ICR;

PP118 - Congenital Hypothyroidism screening program: experience with a TSH lower cutoff in Buenos Aires City.
Autor(es): Vieites A.; Enacan R; Ropelato MG; Gotta G; Dratler G; Junco M; Maccalini G; Micenmacher V.; Aranda C; Chiesa A;

PP119 - Conversion of hypothyroidism by Hashimoto’s Thyroiditis (HT) to hyperthyroidism due to Graves Disease (GD) in a previously healthy child
Autor(es): Costa AP; Fochi, CC; Ali, FR; Ferreira, JCG; Pimentel, SS; Pimentel, SS; Soares,GJB;

PP120 - Differential diagnosis of hepatitis in the course of methimazole treatment.
Autor(es): Pires JVG; Miranda RD; Borges IC; Gomes DC;

PP121 - Differentiated thyroid carcinoma in children and adolescents: Clinical presentation, ATA risk-classification and prognosis
Autor(es): Camassola B; Maccarini J; Caciatori J; Geremia C; Gonçalves I; Puñales M;

PP122 - Diffuse sclerosing variant of papillary thyroid carcinoma, a cause of goitre in a pediatric patient
Autor(es): López LA; Sangri RE; Lopez Perez D.; Benitez FJ; Meixueiro CC; Contreras CV; Gallardo JM;

PP123 - Efficacy of levothyroxine on the frequency and severity of migraine in children with subclinical hypothyroidism
Autor(es): Hayes Dorado JP; Flores Rafael G; Justiniano Vargas G; Quispe Morrore D; Totola Colque DM;

PP124 - Establishment of Reference Intervals for thyrotropin, thyroxine, free thyroxine and triiodothyronine in neonates and infants.
Autor(es): Rodriguez MP; Sobrero GM; Campi V; Martin S; Silvano L; Tarifa C; Testa G; Alloza P; Beltran F; Dichko D; Ochetti M; Muñoz L; Miras M;

PP125 - Follow up of pediatrics patients with Graves Basedow Disease.
Autor(es): Calagua M.; DelAguila C.; Lu R.; Nuñez O.; Chavez E.; Espinoza O.; Pinto P.; DelosSantos M.;

PP126 - HEMITHYROIDECTOMY IN A PEDIATRIC COHORT: THYROID FUNCTION FOLLOW UP
Autor(es): Papendieck P; Masnata ME; Bergada I; Chiesa A;

PP127 - Hypoparathyroidism After Thyroid Surgery: Results From The Mexican Population Registry between 2012-2019
Autor(es): Isabel Galán; Lucia Reyes; Calzada Raul; Arguinzoniz Lissette; Ruiz Maria de la Luz; Diaz Luisa; Hinojosa Carlos;

PP128 - Intrathyroidal ectopic thymus mimicking thyroid nodules in children
Autor(es): Munoz T; De Tezanos-Pinto, A; Moenne K; Ortega X; Hernandez MI;

PP129 - Late diagnosis congenital hypothyroidism and abnormal activity of alpha-L Iduronidase (IDUA)
Autor(es): Mendiola M;

PP130 - Methimazole therapy outcomes in pediatric hyperthyroidism
Autor(es): Ricci J; Morín A; Moreno MR; García Rusca EL; Francesca JS; González VG; Tournier A; Fasano MV; Balbi VA;

PP131 - MUTATION OF THE THYROID HORMONE RECEPTOR AS A CAUSE OF RESISTANCE TO THYROID HORMONE.CASE REPORT
Autor(es): Faries S; Alvarez T; Mejia de Beldjenna L;

PP132 - Mutations in Thyroid Hormone Beta Receptor Gene Identified in Children with Clinical Resistance to Thyroid Hormones
Autor(es): González V.; Balbi V.; Morin A; Reinoso A; Vitale L; Ricci J; Espósito M; Martin R; Tournier A; Adrover E; Molina M; Targovnik H; Rivolta C;

PP133 - NEONATAL SCREENING PROGRAM IN THE CITY OF SANTA CRUZ, BOLIVIA, 10 YEARS OF EXPERIENCE
Autor(es): B. Seoane; C.Siva;

PP134 - Newborn of mothers with Graves´ disease: a case series
Autor(es): Irazusta F; Pintado M; Vidal F; Finozzi MR; Rodriguez MN; Blasina F; Sobrero H;

PP137 - PATIENT’S PROFILE CHARACTERIZATION OF DOWN SYNDROME AND CONGENITAL HYPOTHYROIDISM IN A NEONATAL SCREENING PROGRAM IN SOUTHERN BRAZIL
Autor(es): Rizzotto MIB; Frez DCL; Carreiro S; Vargas PR; Garcia RMR; Castro SM; Kopacek C;



Apresentação Oral Finalistas (em inglês)

OPF1 - Loss-of-function NNT mutations impair antioxidants mechanisms and decreases adrenal steroids secretion in patients with familial glucocorticoid deficieny (FGD)
Autor(es): Bodoni AF; Coeli-Lacchini FB; Sobral LM; Moreira AC; Castro M; Leoplodino AM ; Antonini SR;

OPF2 - MAPK8 activation partially compensates the effects of NNT deficiency in adrenocortical cells
Autor(es): Gebenlian, JL; Bodoni, AF; Coeli-Lacchini, FB; Antonini, SR;

OPF3 - Clinical and genetic aspects of pediatric pheochromocytomas and paragangliomas
Autor(es): Guimaraes AG; Petenuci J; Benedetti AF; Fagundes GFC; Pereira MA; Zerbini MN; Yamauchi F; Srougi V; Tanno FY; Chambo JL; Latronico AC; Mendonca BB; Fragoso MB; Almeida MQ;

OPF4 - Risk alleles of FTO, DRD2 and ANKK1 genes are associated with metabolic risk and have an additive effect on childhood obesity outcome.
Autor(es): Pinto RM; Fortes JS; Monteiro RV; Curado MP; Minasi LB; da Cruz, AD;

OPF5 - T2DRIVE as a new MRI protocol for the diagnosis of Pituitary stalk interruption syndrome (PSIS).
Autor(es): Vieira Peixoto G; Lyra A; Nunes ACB; Gurjão M; Silva TS; Meira AS; Rocha AJ; Longui C; Kochi C;

OPF6 - SEXUAL DIMORPHISM IN THE ASSOCIATION OF BMI TRAJECTORY FROM BIRTH TO EARLY ADULTHOOD WITH CARDIOMETABOLIC RISK IN ADULTHOOD: AN APPROACH USING DYNAMIC PROGRAMMING
Autor(es): CORREA-BURROWS P; ROGAN J; BUNOUT D; BARRERA G; BLANCO E ; GAHAGAN S; BURROWS R;

OPF7 - VALIDITY ASSESSMENT OF THE SINGLE-POINT INSULIN SENSITIVITY ESTIMATOR (SPISE) FOR DIAGNOSIS OF CARDIOMETABOLIC RISK IN 16 YEARS-OLD MALE AND FEMALE ADOLESCENTS.
Autor(es): CORREA-BURROWS P; BLANCO E; GAHAGAN S; BURROWS R;

OPF8 - Burosumab resulted in greater improvement in clinical outcomes than continuation with conventional therapy in younger (1-4 years-old) and older (5-12 years-old) children with X-linked hypophosphatemia (XLH)
Autor(es): Ward LM; Imel EA; Skrinar A; San Martin J;

OPF9 - Clinical and Genetic Characterization of a Constitutional Delay of Growth and Puberty Cohort
Autor(es): Barroso PS; Jorge AAL; Lerario AM; Montenegro LR; Lima-Amato LG; Vasques GA; Silveira LFG; Mendonca BB; Latronico AC;

OPF10 - Predictive Factors, Clinical Characteristics, Reproductive hormones and Growth Factors During Pubertal Transition in Girls with Transient Thelarche
Autor(es): SOTO B. J; MERICQ V.; PEREIRA A.; BUSCH AS; ALMSTRUP K.; Corvalan C.; Juul A.;



Apresentação Pôster Finalistas

PPF1 - Cardio-metabolic risk factors in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Autor(es): Espinosa RT; Valdés GW; Cabrera RJO; Domínguez AE; Pesantez KA; Cordero MD;

PPF2 - EHLERS-DANLOS SYNDROME: MOLECULAR AND CLINICAL CHARACTERIZATION OF TNXA/TNXB CHIMERAS IN CONGENITAL ADRENAL HYPERPLASIA PATIENTS
Autor(es): Marino R; Notaristéfano G; Perez Garrido N; Ramirez P; Touzon MS; Pujana M; Moresco A; Vaiani E; Finkielstain G; Obregón G; Balbi V; Rivarola MA; Belgorosky A;

PPF3 - Synchronization ontogeny between adrenal steroidogenesis genes and circadian rhythm of corticosterone secretion in rats.
Autor(es): Brufatto, J P T; Roa SLR; Antonini SR; Martins CS; Bueno AC; Mermejo LM; Moreira AC;

PPF4 - Response to growth hormone in very young children (<2 years) with growth hormone deficiency compared with prepubertal children aged ≥2 years: data from the NordiNet® International Outcome Study and ANSWER Program
Autor(es): Rohrer T; Ostrow V; Pietropoli A; Berger M; Polak M; Ross J;

PPF5 - IMPACTS ON THE USE OF ZOLENDRONIC ACID IN PATIENTS WITH DIAGNOSIS OF OSTEOGENESIS IMPERFECTA EXPERIENCE IN 18 YEARS.
Autor(es): Orellana-Cárdenas P; Calzada-León R.; Robles-Valdés C.; Altamirano-Bustamante N.; Arguinzoniz-Valenzuela L.; Ruiz-Reyes M; Silva-Camarena M.; Díaz- García L.; Bonilla-Medina P.; Maqueda- Tenorio S.;

PPF6 - CALCITRIOL AS A POTENTIAL THERAPEUTIC OPTION FOR THE TREATMENT OF LEYDIG CELL TUMORS
Autor(es): VARELA ML; ABIUSO AMB; BESIO MORENO M; PIGNATARO OP; BELGOROSKY A; BERENSZTEIN E; MONDILLO C;

PPF7 - BODY MASS INDEX INFLUENCE ON POSTURE OF CHILDREN AND ADOLESCENTS: A BIOPHOTOGRAMMETRY ANALYSIS.
Autor(es): LIMA PLM; Breziniscki MP; Pedrassoli GH; Lacerda Filho L; França SN; Pereira RM; Demartini AC; Kraemer GC; RADOMINSKI RB; FORLIN RB; Carvalho JAR;

PPF8 - NUTRITION, RATHER THAN ETHNICITY AND SOCIOECONOMIC STATUS, CORRELATES WITH AGE OF MENARCHE IN AMAZONIAN GIRLS
Autor(es): Oliveira KC; Antonini SRR; Aragon DC; Cardoso Neto J;

PPF9 - Usefulness of Doppler assessment of the uterine artery for the diagnosis of early sexual development in girl
Autor(es): Silva EFF; Antunes JMV; Antunes OAV; Lima MLLC; Cunha SB; Filgueiras MFTF; Silva IN;

PPF10 - Genetic syndrome and congenital hypothyroidism: profile analysis of patients diagnosed in a neonatal screening reference service after reduction of TSH filter cutoff
Autor(es): Carreiro S; Rizzotto MIB; Garcia RMR; Frez DCL; Castro SM; Kopacek C;





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