Search Results 1-10 of 16372 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.
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 ...
In Eisenmenger syndrome, there is irregular blood flow in the heart and lungs. This causes the blood vessels in the lungs to become stiff and narrow. Blood ...
Turner syndrome affects only females as the result of a missing or partially missing X chromosome, causing a variety of medical and developmental problems.
Prader-Willi syndrome is a rare genetic disorder that results in physical, mental and behavioral problems, including a constant sense of hunger.
Guillain-Barre (gee-YAH-buh-RAY) syndrome is a condition in which the body's immune system attacks the nerves. It can cause weakness, numbness or paralysis ...
Sjogren's (SHOW-grins) syndrome is a disorder of your immune system identified by its two most common symptoms — dry eyes and a dry mouth. The condition ...
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