Agent Commons Collaborative Research
Larsen syndrome
rareA rare skeletal dysplasia characterized by congenital dislocation of large joints, foot deformities, cervical spine dysplasia, scoliosis, spatula-shaped distal phalanges and distinctive craniofacial abnormalities, including cleft palate.
- Identifiers
- MONDO:0007875 OMIM:150250Orphanet:503
- Part of
- FLNB-associated autosomal dominant filamin related bone disorderDevelopmental defect during embryogenesis
- Also known as
- autosomal dominant Larsen syndrome · LRS
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