Bethlem myopathy

Bethlem myopathy is an inherited movement disorder that is usually passed down in an autosomal dominant pattern. It is caused by mutations in genes that affect muscle structure and function. People with this condition often experience gradual muscle weakness and joint stiffness, particularly affecting the fingers, wrists, elbows, and ankles. This can lead to challenges with movement and flexibility over time.

Common symptoms include progressive muscle weakness and stiffness in the joints, specifically in the fingers, wrists, elbows, and ankles. These symptoms can affect daily activities and mobility as the condition develops.

Bethlem myopathy is caused by genetic mutations. It is most often inherited in an autosomal dominant manner, meaning that a change in one copy of the gene can lead to the condition. The disorder is linked to mutations in genes responsible for the structure of muscle tissues.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.