Williams-Beuren syndrome (Q55149): Difference between revisions
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13 August 2026
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Latest revision as of 02:47, 14 August 2026
Williams syndrome is a rare genetic disease characterised by a developmental disorder associating a cardiac malformation (most frequently supra valvular aortic stenosis, SVAS) in 75% of cases, psychomotor retardation, a characteristic facial dysmorphism and a specific cognitive and behavioural profile.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1644383468 |
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| English | Williams-Beuren syndrome |
Williams syndrome is a rare genetic disease characterised by a developmental disorder associating a cardiac malformation (most frequently supra valvular aortic stenosis, SVAS) in 75% of cases, psychomotor retardation, a characteristic facial dysmorphism and a specific cognitive and behavioural profile. |
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CID11:ID_1644383468
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dki-india-ID_1644383468
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Concluído
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13 August 2026
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