hrp0094p2-382 | Pituitary, neuroendocrinology and puberty | ESPE2021

Pituitary tumors in children and adolescents: clinical and etiological profile

Bouichrat Nisrine , Messaoudi Najoua , Zerrouki Dounia , Rouf Siham , Latrech Hanane ,

Introduction: Pituitary tumors are rare in children and adolescents. The etiology is dominated by craniopharyngiomas. The main clinical presentation is the tumoral syndrome. These lesions often affect growth and pubertal development. The objective of our work is to study the clinical and etiological characteristics of pituitary tumors in the pediatric population.Materials and Methods: This is a retrospective descriptive study involving 0...

hrp0095p2-195 | Growth and Syndromes | ESPE2022

Syndromic Disorders with Short Stature

Zerrouki Dounia , Alla Achwak , Rami Imane , Derkaoui Nada , Benyekhlef Salma , Rouf Siham , Latrech Hanane

Keywords: Short stature, Noonan syndrome, Prader-Willi syndrome, Silver-Russell syndrome, genetic syndromesIntroduction: Short stature is one of the major components of dysmorphic syndromes. Growth failure may be due to a wide variety of mechanisms, either related to the growth hormone (GH)/insulin-like growth factor axis or to underlying unknown pathologies. At present, GH therapy is used in most syndromic disorders, al...