Laurin-Sandrow syndrome (Q84233): Difference between revisions
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A síndrome de Laurin-Sandrow é uma síndrome de anomalias do desenvolvimento caracterizada por polissindactilia completa das mãos, pés em espelho e anomalias do nariz (hipoplasia da asa do nariz e columela curta), frequentemente associada a duplicação ulnar e/ou fibular (e às vezes agenesia tibial). | |||
| description / en | description / en | ||
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). | |||
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 |
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| 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). |
