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Results 61 - 70 of 130 for Brain atrophy
  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. AR gene 
    ... 128(Pt 3):659-70. doi: 10.1093/brain/awh381. Epub 2005 Jan 19. Citation on PubMed Beitel LK, Scanlon T, Gottlieb B, Trifiro MA. Progress in Spinobulbar muscular atrophy research: insights into neuronal dysfunction caused by the ...
    https://medlineplus.gov/genetics/gene/ar - Genetics
  7. HSPB8 gene 
    ... characterized by damage to specialized neurons in the brain and spinal cord that control muscle movement (motor neurons). Damage to motor neurons leads to progressive weakness and loss of muscle tissue (atrophy) in the feet and legs. Research suggests that ...
    https://medlineplus.gov/genetics/gene/hspb8 - Genetics
  8. HSPB1 gene 
    ... characterized by damage to specialized neurons in the brain and spinal cord that control muscle movement (motor neurons). Damage to motor neurons leads to progressive weakness and loss of muscle tissue (atrophy) in the feet and legs. HSPB1 gene variants ...
    https://medlineplus.gov/genetics/gene/hspb1 - Genetics
  9. 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
  10. Walker-Warburg syndrome 
    ... inherited disorder that affects development of the muscles, brain, and eyes. It is the most severe of a group of genetic conditions known as congenital muscular dystrophies, which cause muscle weakness and wasting (atrophy) beginning very early in life. The signs and ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
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