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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Detalles Bibliográficos
Autores principales: Dauleh, Hajar, Soliman, Ali, Haris, Basma, Khalifa, Amal, Al Khori, Noor, Hussain, Khalid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959895/
https://www.ncbi.nlm.nih.gov/pubmed/35355562
http://dx.doi.org/10.3389/fendo.2022.826772

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959895/
https://www.ncbi.nlm.nih.gov/pubmed/35355562
http://dx.doi.org/10.3389/fendo.2022.826772

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