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Results 1 - 10 of 10 for Multiple system atrophy
  1. Multiple system atrophy 
    Multiple system atrophy is a progressive brain disorder that affects movement and balance and disrupts the function of the ... pressure. The most frequent autonomic symptoms associated with multiple system atrophy are a sudden drop in blood pressure upon ...
    https://medlineplus.gov/genetics/condition/multiple-system-atrophy - Genetics
  2. Orthostatic hypotension 
    ... as Parkinson's disease, dementia with Lewy bodies, multiple system atrophy, pure autonomic failure, diabetes, Guillain-Barré syndrome, dopamine ...
    https://medlineplus.gov/genetics/condition/orthostatic-hypotension - Genetics
  3. Farber lipogranulomatosis 
    ... to the classic signs, Farber lipogranulomatosis often affects multiple body ... (hydrocephalus), loss (atrophy) of brain tissue, paralysis of the arms and ...
    https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis - Genetics
  4. Dilated cardiomyopathy with ataxia syndrome 
    ... heart problems, movement difficulties, and other features affecting multiple body systems.Beginning in infancy to early childhood, most people ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  5. FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome 
    ... severe condition that begins in infancy and affects multiple body systems. It is primarily associated with brain dysfunction combined ...
    https://medlineplus.gov/...thic-mitochondrial-dna-depletion-syndrome - Genetics
  6. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    ... methylation is abnormal, which affects the expression of multiple genes. Maintenance of the neurons that make up the nervous system is disrupted, leading to the signs and symptoms ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  7. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    ... deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis. Development. 2004 Jan;131(1):3-14. doi: 10.1242/dev.00908. Epub 2003 Nov 26. Citation on PubMed
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  8. Mucopolysaccharidosis type VI 
    ... become inflamed or scarred, and eventually waste away (atrophy). Skeletal ... systems, including skeletal, cardiac, and respiratory.MPS VI causes ...
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-vi - Genetics
  9. Spinocerebellar ataxia type 1 
    ... sensory neuropathy); uncontrolled muscle tensing (dystonia); muscle wasting (atrophy); and muscle twitches (fasciculations). Rarely, rigidity, tremors, and ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  10. Infantile-onset ascending hereditary spastic paralysis 
    ... paraplegia). The spasticity and paraplegia result from degeneration ... areas of the nervous system, affecting the upper limbs and other areas of ...
    https://medlineplus.gov/...et-ascending-hereditary-spastic-paralysis - Genetics