1p36 deletion (Q105605): Difference between revisions
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Revision as of 11:56, 17 August 2026
Monosomy 1p36 is a distinct chromosome deletion syndrome characterised by usually severe developmental delay, behavioural difficulties and self-injury, hypotonia and feeding problems with oropharyngeal dysphagia are frequent, and seizures. Other dysmorphic, cardiac, visual and auditive features have been described.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1248053946 |
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| English | 1p36 deletion |
Monosomy 1p36 is a distinct chromosome deletion syndrome characterised by usually severe developmental delay, behavioural difficulties and self-injury, hypotonia and feeding problems with oropharyngeal dysphagia are frequent, and seizures. Other dysmorphic, cardiac, visual and auditive features have been described. |
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CID11:ID_1248053946
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dki-india-ID_1248053946
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Concluído
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