17p13.3 duplication (Q92848): Difference between revisions
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Revision as of 07:58, 16 August 2026
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.
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| 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. |
