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
Hauptverfasser: Messina, Maria Francesca, Aversa, Tommaso, Mamì, Carmelo, Briuglia, Silvana, Panasiti, Ilenia, De Luca, Filippo, Lombardo, Fortunato
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Sprache:eng
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