hrp0092p3-240 | Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology | ESPE2019

Testicular Regression Syndrome A Clinical and Pathologic Study of 4 Cases

Khlifi Asmaa , Derkaoui Nada , Benyakhlef Salma , Yaden Youssef , Latrech Hanane

Introduction: Testicular regression syndrome (TRS) also called vanishing testes syndrome is a rare developmental disorder that represents less than 5% of cryptorchidism cases. It is characterized by the absence of one or both testicles with partial or complete absence of testicular tissue. TRS phenotypes are various depending on the extent and timing of the intrauterine accident during fetal sexual development.Material and Me...

hrp0094p2-168 | Diabetes and insulin | ESPE2021

Newly-onset type 1 diabetes mellitus triggered by COVID-19: Original case report

Benyakhlef Salma , Abdellaoui Wahiba , Derkaoui Nada , Rouf Siham , Latrech Hanane ,

Introduction: During this year, scientific research revolves around COVID-19, with so many unanswered queries in term of pathogenesis; complications, and mortality rate; in light of limited pediatric evidence. The close relation between COVID 19 and new-onset diabetes especially in children is still an unresolved issue. Our paper, exhibits an unique presentation of DKA misleading COVID 19 diagnosis at this ageCase presentation: A three-y...

hrp0094p2-275 | Growth hormone and IGFs | ESPE2021

Growth hormone therapy in short stature: The variability of responses to treatment after one year. About 41 cases

El Yamani Nada , Abdellaoui Wahiba , Benyakhlef Salma , Rouf Siham , Latrech Hanane ,

Introduction: Growth hormone (GH) therapy has revolutionized the management of patients with short stature. Its common use was first limited to GH deficient children, but now it has been widnened to various other clinical conditions.The aim of our study is to compare the response to GH therapy in patients with GH deficiency (GHD), with those with Turner syndrome and patients small-for-gestational age (SGA).Materials and Methods: We condu...

hrp0094p2-376 | Pituitary, neuroendocrinology and puberty | ESPE2021

Efficacy of cabergoline in the treatment of pituitary macroadenoma complicated in a 14-year-old girl.

Jamal Anouar , Benyakhlef Salma , Aymane Loukili Mohamed , Rbiai Najoua , Rouf Siham , Latrech Hanane ,

Introduction: Pituitary adenomas in children are rare and account for 3% of intracranial tumors in the pediatric population (1), dominated by prolactinomas and corticotropic adenomas, but plurisecreting adenomas are exceptional. We report a case of a 14-year-old girl with a pituitary macroadenoma with a prolactin-predominant plurisecretory immunohistochemical profile revealed by an intracranial hypertension syndrome with a good therapeutic response to cabergol...