19p13.3 microduplication syndrome

MONDO:0018658

19p13.3 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.

Also known as: dup(19)(p13.13)

0 clinical trials for this condition and its sub-types, 0 tagged with 19p13.3 microduplication syndrome itself.

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↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ Partial duplication of the short arm of chromosome 19 (0)

Including sub-types (0) Tagged with 19p13.3 microduplication syndrome (0)

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