Ovotesticular disorder of sexual development and a rare 46,XX/47,XXY karyotype

Ovotesticular disorder of sexual development (DSD) is characterized by the presence of both ovarian and testicular tissues in the same individual. The most common karyotype is 46,XX. Here, we report the case of a boy with a 46,XX/47,XXY karyotype diagnosed as ovotesticular DSD by gonadal biopsy. A 5...

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Veröffentlicht in:	Journal of Pediatric Endocrinology and Metabolism 2013, Vol.26 (7-8), p.789-791
Hauptverfasser:	Ozsu, Elif, Mutlu, Gul Yesiltepe, Cizmecioglu, Filiz M, Ekingen, Gülsen, Muezzinoglu, Bahar, Hatun, Sukru
Format:	Artikel
Sprache:	eng
Schlagworte:	46, XX Disorders of Sex Development - genetics 46, XX Disorders of Sex Development - pathology Humans Infant Karyotype Klinefelter Syndrome - genetics Klinefelter Syndrome - pathology Male Ovotesticular Disorders of Sex Development - diagnosis Ovotesticular Disorders of Sex Development - genetics Ovotesticular Disorders of Sex Development - pathology
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