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Results 21 - 30 of 39 for Brain atrophy
  1. FA2H gene 
    ... that occur in FAHN. Iron accumulation in the brain is probably also ... decline and optic nerve atrophy were said to have a disorder called FA2H- ...
    https://medlineplus.gov/genetics/gene/fa2h - Genetics
  2. DYNC1H1 gene 
    ... thought to contribute to the muscle weakness and atrophy experienced by people with ... have a brain malformation called polymicrogyria. Normally, the surface of the ...
    https://medlineplus.gov/genetics/gene/dync1h1 - Genetics
  3. SEPSECS gene 
    ... Researchers also refer to PCH2D as progressive cerebellocerebral atrophy ... to abnormal brain development in people with PCH2D. More About This ...
    https://medlineplus.gov/genetics/gene/sepsecs - Genetics
  4. SMN1 gene 
    ... gene have been found to cause spinal muscular atrophy. This condition is characterized by a loss of motor neurons that leads to weakness and wasting (atrophy) in muscles used for movement (skeletal muscles) that ...
    https://medlineplus.gov/genetics/gene/smn1 - Genetics
  5. SMN2 gene 
    ... the SMN2 gene do not cause spinal muscular atrophy, but they modify the severity of the disorder. ... motor neurons that leads to weakness and wasting (atrophy) in muscles used for movement (skeletal muscles) that ...
    https://medlineplus.gov/genetics/gene/smn2 - Genetics
  6. GARS1 gene 
    ... a condition called GARS1 infantile-onset spinal muscular atrophy (also known as infantile spinal muscular atrophy, James type). Affected individuals often show weak muscle ...
    https://medlineplus.gov/genetics/gene/gars1 - Genetics
  7. TRPV4 gene 
    ... Tooth disease type 2C, congenital distal spinal muscular atrophy, which is characterized by weakness of muscles in the legs and hips, and scapuloperoneal spinal muscular atrophy, which involves weakness and wasting (atrophy) of muscles ...
    https://medlineplus.gov/genetics/gene/trpv4 - Genetics
  8. ASAH1 gene 
    ... gene have been found to cause spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). This condition is characterized by muscle weakness and wasting (atrophy) and a combination of seizures and uncontrollable muscle ...
    https://medlineplus.gov/genetics/gene/asah1 - Genetics
  9. FHL1 gene 
    ... scapuloperoneal myopathy, X-linked myopathy with postural muscle atrophy (XMPMA), and rigid spine syndrome. Together with Emery- ... DOMINANT; SPM MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMA REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, ...
    https://medlineplus.gov/genetics/gene/fhl1 - Genetics
  10. SMCHD1 gene 
    ... a disorder characterized by muscle weakness and wasting (atrophy) that worsens slowly over time. Two forms of ... these cells, leading to progressive muscle weakness and atrophy.Studies suggest that mutations in the SMCHD1 gene ...
    https://medlineplus.gov/genetics/gene/smchd1 - Genetics
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