Larsen syndrome

MONDO:0007875

A 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.

Also known as: Larsen syndrome, LRS, autosomal dominant Larsen syndrome

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (717) Musculoskeletal system disorder (214) Hereditary disease (188) Bone disorder (51) Human disease (15) Developmental defect during embryogenesis (8) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Skeletal dysplasia (1) Autosomal dominant disease (0)

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