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Results 41 - 50 of 90 for Brain atrophy
  1. 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
  2. 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
  3. 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
  4. 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
  5. Triosephosphate isomerase deficiency 
    ... neurons, which are specialized nerve cells in the brain and spinal cord that control muscle movement. This impairment leads to muscle weakness and wasting (atrophy) and causes the movement problems typical of triosephosphate ...
    https://medlineplus.gov/.../triosephosphate-isomerase-deficiency - Genetics
  6. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    ... of the eye (coloboma), underdevelopment (hypoplasia) or breakdown (atrophy) of the nerves that carry information from the eyes to the brain (optic nerves), or unusually small eyeballs (microphthalmia). These ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  7. Spinal muscular atrophy with progressive myoclonic epilepsy 
    ... the spinal cord and the part of the brain that is connected to the spinal cord (the brainstem). After a few years of normal development, affected children begin experiencing muscle weakness and atrophy in the lower limbs, causing difficulty walking and ...
    https://medlineplus.gov/...rophy-with-progressive-myoclonic-epilepsy - Genetics
  8. Megalencephalic leukoencephalopathy with subcortical cysts 
    ... decreases and the myelin begins to waste away (atrophy). Individuals affected with this condition may develop cysts in the brain; because these cysts form below an area of ...
    https://medlineplus.gov/...eukoencephalopathy-with-subcortical-cysts - Genetics
  9. Fatty acid hydroxylase-associated neurodegeneration 
    ... develop vision problems, which occur due to deterioration (atrophy) of the nerves that carry information from the eyes to the brain (the optic nerves) and difficulties with the muscles ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  10. Infantile-onset ascending hereditary spastic paralysis 
    ... paraplegia). The spasticity and paraplegia result from degeneration (atrophy) of motor neurons, which are specialized nerve cells in the brain and spinal cord that control muscle movement. Hereditary ...
    https://medlineplus.gov/...et-ascending-hereditary-spastic-paralysis - Genetics
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