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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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Detalles Bibliográficos
Autores principales:	Purushothaman, Archana, Larsen, Jennifer
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Endocrine Society 2019
Materias:	Reproductive Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552750/ http://dx.doi.org/10.1210/js.2019-SUN-208

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