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Results 31 - 40 of 90 for Brain atrophy
  1. Autosomal dominant optic atrophy and cataract 
    ... relay visual information from the eyes to the brain (optic nerves), which contributes to vision loss. Atrophy of these nerves causes an abnormally pale appearance ( ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  2. Amyotrophic lateral sclerosis 
    ... are found in the spinal cord and the brain. In ALS, motor neurons die (atrophy) over time, leading to muscle weakness, a loss ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  3. Chorea-acanthocytosis 
    ... this condition worsen with age. Loss of cells (atrophy) in certain brain regions is the major cause of the neurological ...
    https://medlineplus.gov/genetics/condition/chorea-acanthocytosis - Genetics
  4. Autosomal recessive cerebellar ataxia type 1 
    ... progressive problems with movement due to a loss (atrophy) of nerve cells in the part of the brain that coordinates movement (the cerebellum). Signs and symptoms ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  5. Spinal and bulbar muscular atrophy 
    ... the spinal cord and the part of the brain that is connected to the spinal cord (the brainstem).Spinal and bulbar muscular atrophy mainly affects males and is characterized by muscle ...
    https://medlineplus.gov/.../spinal-and-bulbar-muscular-atrophy - Genetics
  6. Gyrate atrophy of the choroid and retina 
    ... affect intelligence; however, abnormalities may be observed in brain imaging or other neurological testing. In some cases, mild to moderate intellectual disability is associated with gyrate atrophy.Gyrate atrophy may also cause disturbances in the ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  7. SLC35A2-congenital disorder of glycosylation 
    ... SLC35A2-CDG, medical imaging shows loss of tissue (atrophy) in parts of the brain called the cerebrum and cerebellum. These brain regions ...
    https://medlineplus.gov/...35a2-congenital-disorder-of-glycosylation - Genetics
  8. 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
  9. 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
  10. 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
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