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Online veröffentlicht: 10. Okt. 2007
Seitenbereich: 51 - 52
DOI: https://doi.org/10.2478/v10034-007-0010-9
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The 46,XX karyotype in a male is a rare sex chromosomal disorder. It mostly results from unequal crossovers between the X and Y chromosomes during meiosis. We here report a 32-year-old infertile male in whom seminal analysis showed azoospermia. Chromosomal analysis revealed a 46,XX karyotype and fluorescent