An unusual case of adolescent type 2 diabetes mellitus: Prader–Willi syndrome

Prader–Willi syndrome (PWS) is a complex genetic disorder, characterized by neonatal hypotonia, developmental delay, short stature, childhood obesity, hypogonadism, and characteristic facial features. Here we report a 21-year-old male who presented with uncontrolled glycemic status. He was diagnosed...

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Detalles Bibliográficos
Autores principales: Basheer, Riyas, Jalal, Muhammed Jasim Abdul, Gomez, Ramesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943134/
https://www.ncbi.nlm.nih.gov/pubmed/27453871
http://dx.doi.org/10.4103/2249-4863.184661

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943134/
https://www.ncbi.nlm.nih.gov/pubmed/27453871
http://dx.doi.org/10.4103/2249-4863.184661

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