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Results 1 - 10 of 19 for Distal weakness
  1. ... Kimber E, Holmgren D, Tulinius M, Oldfors A. Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutation. Neurology. 2007 ...
  2. ... MYH7 gene have been found to cause Laing distal myopathy. This condition causes progressive muscle weakness, particularly affecting the arms and legs. Most of ...
  3. ... gene mutations have been identified in people with distal myopathy, a disorder characterized by weakness and loss of function mainly affecting the muscles ...
  4. ... MATR3 gene has been identified in people with distal myopathy 2, a condition characterized by muscle and vocal cord weakness. The MATR3 gene mutation associated with distal myopathy ...
  5. ... includes Charcot-Marie-Tooth disease type 2C, congenital distal spinal muscular atrophy, which is characterized by weakness of muscles in the legs and hips, and ...
  6. ... DYSF gene mutations also cause another dysferlinopathy called distal myopathy with anterior tibial onset. In this condition, the muscle weakness is most apparent in the muscles of the ...
  7. ... function in a similar way to people with distal hereditary motor neuropathy, type V. This may cause the severe muscle weakness seen in people with GARS1 infantile-onset spinal ...
  8. ... to damage motor neurons, which leads to muscle weakness and the signs and symptoms of distal hereditary motor neuropathy, type V. The same variant ...
  9. ... this gene, the condition is also known as distal anoctaminopathy. Miyoshi myopathy is a muscle disorder that is characterized by progressive weakness and atrophy of muscles that are away from ...
  10. ... mutation that causes a nervous system disorder called distal hereditary motor neuronopathy type VIIB. Signs and symptoms of this disorder first appear in early adulthood and include breathing difficulties and progressive weakness of muscles in the face and hands. Muscle ...
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