The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study

Background Prader-Willi syndrome (PWS) is a complex genetic disorder caused by a deficit in gene expression on the paternal inherited chromosome 15q11.2-q13. It affects various aspects of growth and development, including feeding, cognitive function, and behavior. Early diagnosis and management of P...

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Detalles Bibliográficos
Autores principales: Ahakoud, Mohamed, Daha Belghiti, Hanae, Nedbour, Ayoub, Bouramtane, Abdelhamid, Chaouki, Sana, Bouguenouch, Laila, Ouldim, Karim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202671/
https://www.ncbi.nlm.nih.gov/pubmed/37223137
http://dx.doi.org/10.7759/cureus.37866

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10202671/
https://www.ncbi.nlm.nih.gov/pubmed/37223137
http://dx.doi.org/10.7759/cureus.37866

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