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19p13.3 microduplication syndrome
rare19p13.3 microduplication syndrome is a rare, genetic, syndromic intellectual disability characterized by intrauterine growth retardation, microcephaly, hypotonia, motor and neurodevelopmental delay, speech delay, intellectual disability, and mild dysmorphic features.
- Identifiers
- MONDO:0018658 Orphanet:447980
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial duplication of the short arm of chromosome 19
- Also known as
- dup(19)(p13.13)
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