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Results 1 - 10 of 44 for amyotrophy
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  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. Hereditary neuralgic amyotrophy 
    Hereditary neuralgic amyotrophy is a disorder characterized by episodes of severe pain and muscle wasting (amyotrophy) in one or both shoulders and arms. Neuralgic ...
    https://medlineplus.gov/.../hereditary-neuralgic-amyotrophy - 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. 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
  8. 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
  9. Carpal tunnel syndrome 
    ... feature follows the inheritance pattern of the syndrome. Amyotrophy, thenar, of carpal origin Carpal canal Carpal tunnel ...
    https://medlineplus.gov/genetics/condition/carpal-tunnel-syndrome - Genetics
  10. 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
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