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Results 1 - 10 of 55 for spinal 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 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
  3. 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
  4. 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 ... jerks (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
  5. Spinal muscular atrophy 
    Spinal muscular atrophy is a genetic disorder characterized by weakness and wasting (atrophy) in muscles used for movement (skeletal ... worsens 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 and bulbar muscular atrophy 
    ... 18. Citation on PubMed Finsterer J. Bulbar and spinal muscular atrophy (Kennedy's disease): a review. Eur J Neurol. ... G, Kemp MQ. Androgen receptor and Kennedy disease/spinal bulbar muscular atrophy. Horm Behav. 2008 May;53(5):729-40. ...
    https://medlineplus.gov/.../spinal-and-bulbar-muscular-atrophy - Genetics
  7. Distal hereditary motor neuropathy, type V 
    ... 5 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 
    Distal hereditary motor neuropathy, type II is a progressive disorder that affects nerve cells in the spinal cord. It results in muscle weakness and affects ...
    https://medlineplus.gov/...istal-hereditary-motor-neuropathy-type-ii - Genetics
  9. SMN1 gene 
    ... the SMN1 gene have been found to cause spinal muscular atrophy. This condition is characterized by a loss of ... for 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
  10. SMN2 gene 
    ... copies of the SMN2 gene do not cause spinal muscular atrophy, but they modify the severity of the disorder. ... for movement (skeletal muscles) that worsens with age. Spinal muscular atrophy has a wide range of severity. There are ...
    https://medlineplus.gov/genetics/gene/smn2 - Genetics
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