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SAT-688 Rare Case of 48 XXYY Syndrome with Suspected Type 1 Diabetes Mellitus

BACKGROUND: 48 XXYY syndrome is a rare aneuploidy characterized by the presence of an extra X and Y chromosome in males. Patients share features of Klinefelter syndrome such as tall stature, hypogonadism, congenital malformations and neurocognitive issues. Hypogonadism may cause abdominal adiposity...

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Publicat a:J Endocr Soc
Autors principals: Aftab, Hassaan B, Mirza, Faryal Sardar
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2020
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208577/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.527
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