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Chromosome 17q21.31 duplication syndrome
rareThe newly described 17q21.31 microduplication syndrome is associated with a broad clinical spectrum, of which behavioral disorders and poor social interaction seem to be the most consistent.
- Identifiers
- MONDO:0013298 OMIM:613533Orphanet:217340
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial duplication of the long arm of chromosome 17
- Also known as
- 17q21.31 microduplication syndrome · dup(17)(q21.31) · trisomy 17q21.31
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