Search Results 1-10 of 28286 for Gerstmann syndrome
Changes in a gene called PRNP that makes prion protein cause the genetic forms of the disease. Rare genetic forms also include Gerstmann-Straussler-Scheinker ...
Creutzfeldt-Jakob disease · Frontotemporal dementia; Gerstmann-Straussler-Scheinker syndrome; Hashimoto's encephalopathy; Huntington's disease · Hydrocephalus ...
Learn about this genetic disorder that causes developmental delays, problems with speech and other symptoms.
This complication of an unrepaired congenital heart defect needs close monitoring. Learn how treatment can help manage symptoms and improve quality of life.
In this rare disease, tumors in the digestive tract cause excess production of a certain hormone. High levels of this hormone increase stomach acid, ...
Rett syndrome is a rare genetic neurological and developmental disorder that affects the way the brain develops. This disorder causes a progressive loss of ...
Turner syndrome affects only females as the result of a missing or partially missing X chromosome, causing a variety of medical and developmental problems.
Gerstmann-Straussler-Scheinker syndrome; Giant cell arteritis · Glioblastoma · Glioma; Glossopharyngeal neuralgia; Glycogen storage disease type V (McArdle's ...
Guillain-Barre (gee-YAH-buh-RAY) syndrome is a rare disorder in which your body's immune system attacks your nerves. Weakness and tingling in your hands and ...
Learn about the symptoms and treatment of inflammation of the sac surrounding the heart in post-cardiac injury syndromes.
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