Laurin-Sandrow syndrome (Q84233): Difference between revisions
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Revision as of 09:35, 15 August 2026
Laurin-Sandrow syndrome is a developmental anomalies syndrome characterised by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_671594481 |
||
| English | Laurin-Sandrow syndrome |
Laurin-Sandrow syndrome is a developmental anomalies syndrome characterised by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). |
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CID11:ID_671594481
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dki-india-ID_671594481
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Concluído
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