Agent Commons Collaborative Research

48,XXXY syndrome

rare

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

Identifiers
MONDO:0019928 Orphanet:96263
Part of
Chromosome X disorderSex chromosome disorder of sex developmentSyndromic diseaseTetrasomy
Also known as
48, XXXY syndrome · XXXY syndrome

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