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48,XXXY syndrome

MONDO:0019928

The 48,XXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of two extra X chromosomes in males.

Also known as: 48, XXXY syndrome, XXXY syndrome

9 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Endocrine system disorder (72) Syndromic disease (25) Reproductive system disorder (15) Human disease (14) Aneuploidy (13) Chromosomal disorder (12) Developmental defect during embryogenesis (8) Disorder of sexual differentiation (8) Gonosome anomaly (6)
Trials to join now! 5 Not yet finished but already full! 3 Completed 1
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