19p13.3 microduplication syndrome
Name: |
19p13.3 microduplication syndrome
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Description: |
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.
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ORPHAcode: |
447980
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Synonyms: |
Dup(19)(p13.13)
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
22 Jun 2023 - 16:14
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