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Results 51 - 60 of 130 for Brain atrophy
  1. Spastic paraplegia type 15 
    ... connecting the left and right halves of the brain (corpus callosum) is abnormally thin and becomes thinner over time. Additionally, there is often a loss (atrophy) of nerve cells in several parts of the ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-15 - Genetics
  2. Spinal muscular atrophy 
    ... Muscles cannot contract without receiving signals from the brain, so many skeletal muscles become weak and waste away, leading to the signs and symptoms of spinal muscular atrophy.Typically, people have two copies of the SMN1 ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  3. TPM3 gene 
    ... Nonaka I. The significance of type 1 fiber atrophy (hypotrophy) in childhood neuromuscular disorders. Brain Dev. 2001 Aug;23(5):298-302. doi: ...
    https://medlineplus.gov/genetics/gene/tpm3 - Genetics
  4. Boucher-Neuhäuser syndrome 
    ... syndrome, it arises from a loss of cells (atrophy) in the part of the brain involved in coordinating movements (the cerebellum). Affected individuals ...
    https://medlineplus.gov/.../condition/boucher-neuhauser-syndrome - Genetics
  5. BICD2 gene 
    ... KN. Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2. Brain. 2015 Feb;138(Pt 2):293-310. doi: ...
    https://medlineplus.gov/genetics/gene/bicd2 - Genetics
  6. Spinal muscular atrophy with lower extremity predominance 
    ... KN. Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2. Brain. 2015 Feb;138(Pt 2):293-310. doi: ...
    https://medlineplus.gov/...atrophy-with-lower-extremity-predominance - Genetics
  7. Congenital fiber-type disproportion 
    ... Nonaka I. The significance of type 1 fiber atrophy (hypotrophy) in childhood neuromuscular disorders. Brain Dev. 2001 Aug;23(5):298-302. doi: ...
    https://medlineplus.gov/.../congenital-fiber-type-disproportion - Genetics
  8. TPP1 gene 
    ... People with SCAR7 have progressive loss of cells (atrophy) of various parts of the brain, particularly within the cerebellum, which is the area ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  9. Fukuyama congenital muscular dystrophy 
    ... an inherited condition that predominantly affects the muscles, brain, and eyes. Congenital muscular dystrophies are a group of genetic conditions that cause muscle weakness and muscle wasting (atrophy) beginning early in life. The signs and symptoms ...
    https://medlineplus.gov/.../fukuyama-congenital-muscular-dystrophy - Genetics
  10. 3-methylglutaconyl-CoA hydratase deficiency 
    ... These individuals have damage to a type of brain tissue called white matter ... optic atrophy, and a decline in intellectual function (dementia).Affected ...
    https://medlineplus.gov/...methylglutaconyl-coa-hydratase-deficiency - Genetics
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