Marden-Walker syndrome (Q85066): Difference between revisions
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Revision as of 10:25, 15 August 2026
Marden-Walker syndrome is a developmental anomalies syndrome characterised by multiple congenital joint contractures, dysmorphic features with a mask-like face, blepharophimosis, ptosis, micrognathia, cleft or high-arched palate, low-set ears, arachnodactyly, decreased muscular mass, failure to thrive and psychomotor retardation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1983460876 |
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| English | Marden-Walker syndrome |
Marden-Walker syndrome is a developmental anomalies syndrome characterised by multiple congenital joint contractures, dysmorphic features with a mask-like face, blepharophimosis, ptosis, micrognathia, cleft or high-arched palate, low-set ears, arachnodactyly, decreased muscular mass, failure to thrive and psychomotor retardation. |
