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Autosomal dominant brachyolmia

rare

Autosomal dominant brachyolmia is a relatively severe form of brachyolmia, a group of rare genetic skeletal disorders, characterized by short-trunked short stature, platyspondyly and kyphoscoliosis. Degenerative joint disease (osteoarthropathy) in the spine, large joints and interphalangeal joints becomes manifest in adulthood.

Causal genes
TRPV4
Also known as
BCYM3 · brachyolmia autosomal dominant · brachyolmia type 3 · brachyolmia, autosomal dominant

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