Treatment of a Prader-Willi Patient with Recurrent Catatonia

Prader-Willi is a genetic disorder characterized by neonatal hypotonia, hyperphagia, short stature, hypogonadism, and mental delay. This disorder can result from multiple mechanisms, most commonly a deletion of paternal chromosome 15, leaving a single maternally derived chromosome 15. Individuals wh...

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Detalles Bibliográficos
Autores principales: Poser, Hana M., Trutia, Alexandru E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439498/
https://www.ncbi.nlm.nih.gov/pubmed/26064753
http://dx.doi.org/10.1155/2015/697428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439498/
https://www.ncbi.nlm.nih.gov/pubmed/26064753
http://dx.doi.org/10.1155/2015/697428

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