Autosomal dominant brachyolmia
MONDO:0007232Autosomal 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.
Also known as: brachyolmia type 3, brachyolmia, autosomal dominant, BCYM3, brachyolmia autosomal dominant, brachyrachia
35 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials