Laurin-Sandrow syndrome

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Revision as of 14:58, 3 February 2021 by Deepika vegiraju (talk | contribs) (Created page with "== '''Alternate names''' == Fibula ulna duplication tibia radius absence; Sandrow syndrome; Mirror hands and feet with nasal defects; Tetramelic mirror-image polydactyly; Laur...")
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Alternate names[edit]

Fibula ulna duplication tibia radius absence; Sandrow syndrome; Mirror hands and feet with nasal defects; Tetramelic mirror-image polydactyly; Laurin Sandrow syndrome

Definition[edit]

Laurin-Sandrow syndrome (LSS) is 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). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported, and may represent the same entity. The etiology of LSS is unknown. Different modes of inheritance have been suggested.

NIH genetic and rare disease info[edit]

Laurin-Sandrow syndrome is a rare disease.

Rare and genetic diseases

Rare diseases - Laurin-Sandrow syndrome

A-Z list of rare diseases
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