Case Report: Hepatic Adenomatosis in a Patient With Prader–Willi Syndrome

Prader–Willi syndrome (PWS) is a genetic disorder caused by the lack of expression of genes on the paternally inherited chromosome region 15q11.2-q13. It is a multisystem disorder that is characterized by severe hypotonia with poor suck and feeding difficulties in early infancy, followed in early ch...

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Bibliographic Details
Main Authors: Hajar Dauleh, Ali Soliman, Basma Haris, Amal Khalifa, Noor Al Khori, Khalid Hussain
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-03-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2022.826772/full