Ambiguous genitalia in a 48, XXYY newborn: a casual relationship or a coincidence?
48, XXYY is a very rare sex chromosome aneuploidy, characterized by both an extra X and Y chromosome with a prevalence of 1:18,000-1:40,000. Most patients are diagnosed prenatally by cytogenetic examination of amniotic fluid, or during the first years of life because of severe developmental delay, c...
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Veröffentlicht in: | Journal of Pediatric Endocrinology and Metabolism 2013, Vol.26 (9-10), p.921-923 |
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