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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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| Pubblicato in: | J Endocr Soc |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2020
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| Soggetti: | |
| Accesso online: | 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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