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48,XXYY syndrome

MONDO:0015028

The 48,XXYY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of an extra X and Y chromosome in males.

Also known as: 48, XXYY Syndrome, 48, XXYY syndrome, 48,XXYY Klinefelter syndrome, 48,XXYY variant of Klinefelter's syndrome, XXYY syndrome

5 clinical trials for this condition and its sub-types, 0 tagged with 48,XXYY syndrome itself.

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Part of

↑ Syndromic disease (7158) ↑ Sex chromosome disorder of sex development (34)
Including sub-types (5) Tagged with 48,XXYY syndrome (0)
Trials to join now! 4 Not yet finished but already full! 1
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