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Results 1 - 10 of 142 for Muscular atrophy
  1. Spinal muscular atrophy with lower extremity predominance 
    Spinal muscular atrophy with lower extremity predominance (SMA-LED) is characterized by muscle weakness and wasting (atrophy) in the lower limbs, most severely ...
    https://medlineplus.gov/...atrophy-with-lower-extremity-predominance - Genetics
  2. Spinal and bulbar muscular atrophy 
    Spinal and bulbar muscular atrophy, also known as Kennedy disease, is a disorder of specialized nerve cells that control muscle movement (motor neurons). These ...
    https://medlineplus.gov/.../spinal-and-bulbar-muscular-atrophy - Genetics
  3. Spinal muscular atrophy with respiratory distress type 1 
    Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is an inherited condition that causes muscle weakness and respiratory failure typically beginning ...
    https://medlineplus.gov/...-atrophy-with-respiratory-distress-type-1 - Genetics
  4. X-linked infantile spinal muscular atrophy 
    X-linked infantile spinal muscular atrophy is a condition that affects only boys and is characterized by severe muscle weakness and absent reflexes (areflexia). ...
    https://medlineplus.gov/...-linked-infantile-spinal-muscular-atrophy - Genetics
  5. Spinal muscular atrophy 
    Spinal muscular atrophy is a genetic disorder characterized by weakness and wasting (atrophy) in muscles used for movement (skeletal muscles). ... with age. There are many types of spinal muscular atrophy that are caused by changes in the same ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  6. Spinal muscular atrophy with progressive myoclonic epilepsy 
    Spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME) is a neurological condition that begins in childhood. SMA-PME causes ... myoclonic epilepsy).In individuals with SMA-PME, spinal muscular atrophy results from a loss of specialized nerve cells, ...
    https://medlineplus.gov/...rophy-with-progressive-myoclonic-epilepsy - Genetics
  7. Distal hereditary motor neuropathy, type V 
    ... Distal hereditary motor neuronopathy, type V Distal spinal muscular atrophy, type V DSMAV HMN V Spinal muscular atrophy, distal type V Spinal muscular atrophy, distal, with ...
    https://medlineplus.gov/...distal-hereditary-motor-neuropathy-type-v - Genetics
  8. Distal hereditary motor neuropathy, type II 
    ... years, affected individuals experience a gradual loss of muscle tissue (atrophy) in the lower legs. They begin to have trouble walking and running, and eventually may have complete paralysis of the lower legs. The thigh muscles may also be affected, although generally this occurs ...
    https://medlineplus.gov/...istal-hereditary-motor-neuropathy-type-ii - Genetics
  9. Myotonic dystrophy 
    Myotonic dystrophy is part of a group of inherited disorders called muscular dystrophies. It is the most common form of muscular dystrophy that begins in adulthood. ...
    https://medlineplus.gov/genetics/condition/myotonic-dystrophy - Genetics
  10. SMN1 gene 
    ... SMN1 gene have been found to cause spinal muscular atrophy. This condition is characterized by a loss of ... movement (skeletal muscles) that worsens with age. Spinal muscular atrophy has a wide range of severity. There are ...
    https://medlineplus.gov/genetics/gene/smn1 - Genetics
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