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Results 1 - 10 of 13 for Parkinson disease 10
  1. Parkinson's disease 
    ... Testing Registry: Parkinsonian-pyramidal syndrome Genetic Testing Registry: Parkinson disease 10 Genetic Testing Registry: Parkinson disease 12 Genetic Testing ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  2. Wolff-Parkinson-White syndrome 
    ... 300. Citation on PubMed Light PE. Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction? J Cardiovasc Electrophysiol. 2006 May;17 Suppl 1:S158-S161. doi: 10.1111/j.1540-8167.2006.00399.x. Citation ...
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  3. Essential tremor 
    ... than average risk of developing neurological conditions including Parkinson's disease or sensory problems such as hearing loss, especially in individuals whose tremor appears after age 65. Essential tremor is a common disorder, affecting up to 10 million people in the United States. Estimates of ...
    https://medlineplus.gov/genetics/condition/essential-tremor - Genetics
  4. Tyrosine hydroxylase deficiency 
    ... symptoms may resemble those seen in people with Parkinson disease: stiffness of the muscles in the arms and ...
    https://medlineplus.gov/.../tyrosine-hydroxylase-deficiency - Genetics
  5. Infantile neuroaxonal dystrophy 
    ... as the more common Alzheimer's disease and Parkinson's disease, also are associated with changes in brain iron ... iron accumulation, PLA2G6-related Seitelberger disease Seitelberger's disease ... neuroaxonal dystrophy but not dystonia-parkinsonism. PLoS One. 2010 Sep 23;5(9):e12897. doi: 10.1371/journal.pone.0012897. Citation on PubMed or ...
    https://medlineplus.gov/.../infantile-neuroaxonal-dystrophy - Genetics
  6. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    ... sclerosis and progressive problems with movement and balance (Parkinson's disease).People with IBMPFD usually live into their fifties ... in four families: hereditary inclusion body myopathy, Paget disease of bone, and ... doi: 10.1006/mgme.2001.3256. Citation on PubMed Nalbandian ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  7. Restless legs syndrome 
    ... disease, diabetes mellitus, multiple sclerosis, rheumatoid arthritis, and Parkinson's disease. People with low iron levels associated with a ...
    https://medlineplus.gov/genetics/condition/restless-legs-syndrome - Genetics
  8. Intestinal pseudo-obstruction 
    ... or nerves in the intestinal tract, such as Parkinson's disease, type 2 diabetes, various types of muscular dystrophy, ... article on PubMed Central Kapoor S. Kawasaki's disease: an often ... Arch. 2015 Nov;467(5):619-20. doi: 10.1007/s00428-015-1844-2. Epub 2015 Sep ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics
  9. Congenital mirror movement disorder 
    ... life in people with neurodegenerative disorders such as Parkinson's disease. Mirror movements may also be present in certain ...
    https://medlineplus.gov/.../congenital-mirror-movement-disorder - Genetics
  10. Orthostatic hypotension 
    ... occurs along with nervous system disorders such as Parkinson's disease, dementia with Lewy bodies, multiple system atrophy, pure ...
    https://medlineplus.gov/genetics/condition/orthostatic-hypotension - Genetics
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