A5064503942- Sexual Differentiation and Disorders
- Surgical Simulation and Training
- Urological Disorders and Treatments
- Congenital gastrointestinal and neural anomalies
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Ovarian cancer diagnosis and treatment
- Hormonal and reproductive studies
- Gynecological conditions and treatments
- Gastrointestinal disorders and treatments
- Anatomy and Medical Technology
- Congenital Diaphragmatic Hernia Studies
- Congenital Anomalies and Fetal Surgery
- Intestinal Malrotation and Obstruction Disorders
- Testicular diseases and treatments
- Pediatric Hepatobiliary Diseases and Treatments
- Pelvic floor disorders treatments
- Pediatric Urology and Nephrology Studies
- Urologic and reproductive health conditions
- Esophageal and GI Pathology
- Uterine Myomas and Treatments
- Gallbladder and Bile Duct Disorders
- Central Venous Catheters and Hemodialysis
- Cerebrospinal fluid and hydrocephalus
- Teratomas and Epidermoid Cysts
- Female Genital Mutilation/Cutting Issues
Garrahan Hospital
2014-2024
The Spine Institute
2022
Instituto Nacional de Pediatria
2020
University of Buenos Aires
2017-2019
Children's Hospital
2018
Juntendo University Nerima Hospital
2018
American College of Surgeons
2016
Hospital Británico de Buenos Aires
2013
Boston Children's Hospital
2010
Hospital Alemán
2005-2008
No AccessJournal of Urology1 Aug 1992Vaginal Reconstruction after Initial Construction the External Genitalia in Girls With Salt-Wasting Adrenal Hyperplasia M.M. Bailez, John P. Gearhart, Claude Migeon, and Rock BailezM.M. Bailez More articles by this author , GearhartJohn Gearhart MigeonClaude Migeon RockJohn View All Author Informationhttps://doi.org/10.1016/S0022-5347(17)36691-0AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked...
<i>Background:</i> Three novel heterozygous SF-1 gene mutations affecting multiple members of two unrelated families with a history 46,XY disorders sex development (DSD) and 46,XX ovarian insufficiency are described. <i>Methods:</i> Clinical mutational analysis the in 9 subjects families. <i>Results:</i> Family 1 had 2 affected DSD subjects. One, born severe perineal hypospadias, was raised as male, presented normal adolescence. The other, ambiguous...
Summary Background IGF1R gene mutations have been associated with varying degrees of intrauterine and postnatal growth retardation, microcephaly. Objective To identify characterize variations in a cohort 28 Argentinean children suspected having IGF ‐1 insensitivity, who were selected on the basis association pre/postnatal failure Methods The coding sequence flanking intronic regions amplified directly sequenced. Functional characterization was performed by two vitro assays: 1) [Methyl‐ 3 H]...
Aim :Evaluate postoperative urinary continence in patients withcongenital adrenal hyperplasia(CAH)with intermediate (IT)and high urogenital sinus (UGS) who underwent a UGS mobilization maneuver . Methods: We called IT to those that although needing an aggressive dissection get the vagina, still have enough urethra proximal vaginal confluence. Very low variants are excluded from this analysis. Dissection always started posterior wall of with separation anterior rectal wall. If wide portion...
Objective To assess if application of fibrin glue sealant to the peritoneal cuff suture is useful in prevention early dialysate leakage children with end-stage renal disease on chronic dialysis (CPD). Design Single-center, open-label, prospective randomized study. Setting University Pediatric Hospital. Methods 52 catheters were implanted 45 (mean age 6.2 ± 4.5 years). Catheters randomly assigned either control group or group. In latter group, 1 mL was applied suture. 18 used for first time...
The aim of this report was to present our experience with a modified surgical technique designed for the treatment choledochal cysts (CC) in children.Between June 2004 and February 2005, we operated on 6 patients diagnosis type I CC by means "leak-free" that consists transient complete sealing hepatic duct duration dissection, single- or double laparoscopic running suture build end-to-side hepatico-jejuno anastomosis. There were 4 females 2 males, whose age ranged between 45 days 7 years...
Context:Steroid acute regulatory (StAR) protein is a mitochondria-targeted that part of the transduceosome complex crucial for transport cholesterol to mitochondria. Recessive mutations cause classic and nonclassic congenital lipoid adrenal hyperplasia.
Androgen insensitivity syndrome (AIS) is a hereditary condition in patients with 46,XY karyotype which loss-of-function mutations of the androgen receptor (<i>AR</i>) gene are responsible for defects virilization. The aim this study was to investigate consequences lack AR activity on germ cell survival and degree testicular development reached by these analyzing gonadal tissue from AIS prior Sertoli maturation at puberty. Twenty-three gonads 13 were assessed compared 18 testes 17...
Tailgut cyst (TGC) is an uncommon congenital lesion, located in the retrorectal/presacral space. We report a 12-year-old girl with lumbar pain and retrorectal mass. She had mental retardation, hypothyroidism, didelphus uterus, sacrum vertebrae, coccyx agenesis, without chromosomic anomalies. Three surgeries were performed for complete excision of tumor. Microscopically, mass consisted cystic spaces lined by wide variety epithelia stroma composed fibrous tissue containing bundles smooth...