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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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| Udgivet i: | J Family Med Prim Care |
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| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Medknow Publications & Media Pvt Ltd
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4943134/ https://ncbi.nlm.nih.gov/pubmed/27453871 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2249-4863.184661 |
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