A rare occurrence of non-classic congenital adrenal hyperplasia and type 1 diabetes mellitus in a girl with Prader-Willi Syndrome: Case report and review of the literature

A rare occurrence of non-classic congenital adrenal hyperplasia and type 1 diabetes mellitus in a girl with Prader-Willi Syndrome: Case report and review of the literature

Prader–Willi syndrome (PWS) is a rare genetic disorder resulting from lack of expression of the paternally derived chromosome 15q11–13, associated with several complications, including pubertal disorders, short stature, hyperphagia, obesity, glucose metabolism abnormalities, scoliosis, obstructive s...

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Bibliographic Details
Main Authors: Alessia Aureli, Sarah Bocchini, Michela Mariani, Antonino Crinò, Marco Cappa, Danilo Fintini
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-04-01
Series:Frontiers in Endocrinology
Subjects:
Prader-Willi Syndrome
adrenarche
premature pubarche
pubertal development
growth hormone deficiency
congenital adrenal hyperplasia
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2023.1148318/full

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