Laurin-Sandrow syndrome (Q84233): Difference between revisions

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Latest 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).