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Up to: Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Partial duplication of the short arm of chromosome 19
19p13.3 microduplication syndrome
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.
This condition has no sub-types.