Search Results 21-30 of 27701 for Huntington's+disease
Mayo Clinic researchers identified the first MAPT gene mutations for a behavioral form of dementia in 1998, and other genetic changes associated with related ...
Brain tumor; Cerebral palsy; Guillain-Barre syndrome; Head injury; Huntington's disease; Lyme disease; Multiple sclerosis; Muscular dystrophy; Myasthenia gravis ...
Hirschsprung's (HIRSH-sproongz) disease is a condition that affects the large intestine (colon) and causes problems with passing stool.
The inherited disease is linked to a mutation in the ATXN3 gene. This mutation, which affects the central nervous system, appears between the ages of 40 and 70, ...
High levels of the hormone cortisol in your body cause this endocrine disorder. Learn about symptoms, causes and treatment.
Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. In muscular dystrophy, abnormal genes (mutations) ...
This complication of an unrepaired congenital heart defect needs close monitoring. Learn how treatment can help manage symptoms and improve quality of life.
The Neurobiology of Parkinson's Disease Lab studies mechanisms of neurodegeneration in Parkinson's disease, Lewy body dementia & related synucleinopathies.
... disease conditions in Alzheimer's disease, Parkinson's disease, Huntington's disease, multiple sclerosis, metabolic disorders and aging. These approaches ...
This inherited blood vessel disorder can cause severe nosebleeds, strokes, bleeding in the digestive tract and anemia.
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