Prader-Willi Syndrome and Schaaf-Yang Syndrome: Neurodevelopmental Diseases Intersecting at the MAGEL2 Gene

Prader-Willi syndrome (PWS) is a neurodevelopmental disorder characterized by neonatal hypotonia, developmental delay/intellectual disability, and characteristic feeding behaviors with failure to thrive during infancy; followed by hyperphagia and excessive weight gain later in childhood. Individuals...

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Detalles Bibliográficos
Autores principales: Fountain, Michael D., Schaaf, Christian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456300/
https://www.ncbi.nlm.nih.gov/pubmed/28933382
http://dx.doi.org/10.3390/diseases4010002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456300/
https://www.ncbi.nlm.nih.gov/pubmed/28933382
http://dx.doi.org/10.3390/diseases4010002

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