Searchable abstracts of presentations at key conferences in endocrinology

ea0095p47 | Gonadal, DSD and Reproduction 1 | BSPED2023

A rare cause of gonadal dysgenesis due to TOE1 gene mutation

ibrahim Mohsina Noor , Yasir Meherunnisa , Khan Yasirnaqi , Chachar Saadullah , Parveen Roshia , Riaz Maira , Rai Versha

Introduction: 46XY gonadal dysgenesis is one of the important cause of DSD with varied clinical presentation Genetic mutations like SRY, NR5A1, SOX9, DHX37 are common mutations that can cause gonadal dysgenesis. Genetic testing for reaching final diagnosis in 46 XY DSD is increasingly playing a crucial role in the management plan.Case: A 10-month-old patient presented in our DSD clinic with complaint of atypical genitali...