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Results 1 - 10 of 23 for Progressive distal muscle weakness
  1. MYH7 gene 
    ... the structure and function of myosin lead to progressive muscle weakness in people with Laing distal myopathy. More About This Health Condition At least ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  2. Laing distal myopathy 
    ... unknown how mutations in the MYH7 gene cause progressive muscle weakness in people with Laing distal myopathy. Researchers have proposed that these mutations alter ...
    https://medlineplus.gov/genetics/condition/laing-distal-myopathy - Genetics
  3. ANO5 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/ano5 - Genetics
  4. Troyer syndrome 
    ... include delays in learning to walk and talk, progressive weakness and spasticity of the leg muscles, muscle wasting in the hands and feet (distal amyotrophy), and short stature. Affected individuals may also ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  5. DYSF gene 
    ... is a muscle disorder that is characterized by progressive weakness and atrophy of muscles that are away from the center of the body (distal muscles), particularly those in the legs. The DYSF ...
    https://medlineplus.gov/genetics/gene/dysf - Genetics
  6. HSPB1 gene 
    ... motor neurons). Damage to motor neurons leads to progressive weakness and loss of muscle tissue (atrophy) in the feet and legs. HSPB1 gene variants are the most common cause of distal hereditary motor neuropathy, type II. The HSPB1 gene ...
    https://medlineplus.gov/genetics/gene/hspb1 - Genetics
  7. Distal hereditary motor neuropathy, type II 
    Distal hereditary motor neuropathy, ... over time. Distal hereditary motor neuropathy, type II weakness primarily affects ...
    https://medlineplus.gov/...istal-hereditary-motor-neuropathy-type-ii - Genetics
  8. DMPK gene 
    ... dystrophy type 1. Myotonic dystrophy is characterized by progressive muscle wasting and weakness. The muscle weakness associated with type 1 particularly affects muscles farthest from the center of the body (distal muscles), such as those of the lower legs, ...
    https://medlineplus.gov/genetics/gene/dmpk - Genetics
  9. DCTN1 gene 
    ... 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 weakness in ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
  10. HSPB8 gene 
    ... have been found to cause a condition called distal hereditary motor ... leads to progressive weakness and loss of muscle tissue (atrophy) in the ...
    https://medlineplus.gov/genetics/gene/hspb8 - Genetics
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