46, XX man with SRY gene translocation: cytogenetic characteristics, clinical features and management - PubMed (original) (raw)
Case Reports
46, XX man with SRY gene translocation: cytogenetic characteristics, clinical features and management
Ali A Rizvi. Am J Med Sci. 2008 Apr.
Abstract
This report describes a well-masculinized 33-year-old man with infertility and primary hypogonadism in whom chromosomal evaluation revealed a 46, XX karyotype. This syndrome is a rare but important cause of hypergonadotropic hypogonadism in which the diagnosis can be delayed or missed. A review of the cytogenetic basis and clinical features is presented to raise awareness of this entity among clinicians and to emphasize the importance of appropriate laboratory testing when indicated.
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