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GTR Home > Conditions/Phenotypes > Laurin-Sandrow syndrome

Laurin-Sandrow syndrome

Synonyms
FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUS; Fibula ulna duplication tibia radius absence; Mirror hands and feet with nasal defects; Sandrow syndrome; Tetramelic mirror-image polydactyly
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

Laurin-Sandrow syndrome (LSS) is an autosomal dominant disorder characterized by polysyndactyly of hands and feet, mirror image duplication of feet, and nasal defects (hypoplastic alae nasi, short columella), in connection with absent patella and duplicated fibula (summary by Lohan et al., 2014). [from OMIM]

Available tests

9 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (9 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ACHP, C7orf2, DIF14, LSS, PPD2, THYP, TPT, TPTPS, ZRS, LMBR1
    Summary: limb development membrane protein 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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