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Results 1 - 9 of 9 for Parkinson "Disease," Dominant
  1. Parkinson's disease 
    ... disease PD Primary parkinsonism Genetic Testing Registry: Autosomal dominant Parkinson disease 1 Genetic Testing Registry: Autosomal dominant Parkinson disease ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  2. LRRK2 gene 
    ... A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet. 2005 Jan 29-Feb 4;365(9457): ...
    https://medlineplus.gov/genetics/gene/lrrk2 - Genetics
  3. Essential tremor 
    ... from other disorders or known causes, such as Parkinson's disease or head trauma. Essential tremor usually occurs alone, ... than average risk of developing neurological conditions including Parkinson's disease or sensory problems such as hearing loss, especially ...
    https://medlineplus.gov/genetics/condition/essential-tremor - Genetics
  4. 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 ... on PubMed Central Kimonis VE, Watts GD. Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. Alzheimer Dis Assoc ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  5. Restless legs syndrome 
    ... disease, diabetes mellitus, multiple sclerosis, rheumatoid arthritis, and Parkinson's disease. People with low iron levels associated with a ... have an autosomal dominant pattern of inheritance. Autosomal dominant inheritance suggests that one copy of an altered gene in ... ClinicalTrials.gov ...
    https://medlineplus.gov/genetics/condition/restless-legs-syndrome - Genetics
  6. 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
  7. Intestinal pseudo-obstruction 
    ... or nerves in the intestinal tract, such as Parkinson's disease, type 2 diabetes, various types of muscular dystrophy, ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics
  8. 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 ...
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  9. CHMP2B-related frontotemporal dementia 
    ... unclear why the signs and symptoms of this disease are related primarily to the frontal and temporal lobes. CHMP2B This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../chmp2b-related-frontotemporal-dementia - Genetics