17p13.3 duplication (Q92848)
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17p13.3 microduplication syndrome is a chromosomal anomaly characterised by a common clinical spectrum comprising mild to moderate psychomotor delay, hypotonia and discrete craniofacial dysmorphic features including a high forehead with frontal bossing, a small nose and a small mouth.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_288421473 |
||
| English | 17p13.3 duplication |
17p13.3 microduplication syndrome is a chromosomal anomaly characterised by a common clinical spectrum comprising mild to moderate psychomotor delay, hypotonia and discrete craniofacial dysmorphic features including a high forehead with frontal bossing, a small nose and a small mouth. |
Statements
CID11:ID_288421473
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