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SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
Introduction: Klinefelter syndrome (KS) is the most common X chromosome abnormality and genetic cause of male infertility. Nondisjunction of paired X chromosomes during meiosis or gametogenesis gives rise to the karyotype 47XXY seen in 80 % of cases. The most common form of mosaicism results from po...
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| Publié dans: | J Endocr Soc |
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| Auteurs principaux: | , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Endocrine Society
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6552750/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-208 |
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