Abstract
With the advancement of medical care, the survival of most patients with syndromal genetic disease is greatly improved. In this case report, we have reported an adult Prader-Willi syndrome patient who is being diagnosed at the age of 33. The clinical features and their associated complications during adulthood have been reviewed.
Cite
CITATION STYLE
APA
Ho-Ming, L. (2016). Adult Prader-Willi Syndrome: An Update on Management. Case Reports in Genetics, 2016, 1–3. https://doi.org/10.1155/2016/5251912
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