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- ... cause the disorder. In some cases, an affected person inherits the mutation from one affected parent. Other ... the disorder. Congenital stiff-man syndrome Congenital stiff-person syndrome Familial hyperekplexia Hyperekplexia Startle syndrome STHE Stiff- ...
- ... fructose intolerance is a condition that affects a person's ability to digest the sugar fructose. Fructose ...
- ... a psychosis, which means that it affects a person's thinking, sense of self, and perceptions. The ...
- Congenital sucrase-isomaltase deficiency is a rare genetic disorder that affects an individual's ability to digest certain sugars. People with this condition cannot ...
- ... of these symptoms does not mean that a person definitely has breast cancer.In some cases, cancerous ... cancer, these genetic changes are acquired during a person's lifetime and are present only in certain ...
- ... in the blood. Too much cholesterol increases a person's risk of developing heart disease.People with ... chest pain called angina and greatly increases a person's risk of having a heart attack.Familial ...
- ... cancer, these genetic changes are acquired during a person's lifetime and are present only in certain ... with non-genetic factors, also influence whether a person will develop parathyroid cancer.Mutations in the CDC73 ...
- ... of daily living. Even in familiar settings, a person with Alzheimer's disease may get lost or ... of the early-onset form appear between a person's thirties and mid-sixties, while the late- ...
- ... be focused and the more severely nearsighted a person will be.Nearsightedness is measured by how powerful ... used to correct nearsightedness. The more severe a person's nearsightedness, the larger the number of diopters ...
- ... signs and symptoms of the condition vary from person to person.Tuberous sclerosis complex often affects the brain, with ... TSC2 gene must occur in cells during a person's lifetime.Cells that have variants in both ...