Gerstmann-Sträussler-Scheinker disease (GSS) is a hereditary form of prion disease caused by mutations in the PRNP gene. It is characterized by progressive neurodegeneration, ataxia, and dementia. Symptoms typically manifest in adulthood.
Excessive bleeding when a cut or other abrasive injury occurs
Carriers of the gene for hereditary fructose intolerance can be identified through DNA analysis. Anyone who is known to carry the disease or who has the disease in his or her family can benefit from genetic counseling.
A pathogen is any infectious agent (parasite, bacteria, virus, fungus, etc.) that causes a disease to its host, the body it affects. Any disease caused by a foreign, biological agent is considered a pathogenic disease. Examples include: tetanus(bacteria), influenza(virus).
With the exception of bacteria cells, hereditary material is held in the cell's nucleus.
This disease is known as Narcolepsy.
no albinism is a hereditary.
Orthopnea is not hereditary. It is a symptom of a disease.
Gayness
The disease was hereditary in their family.
In about 8-12% of cases, people diagnosed with narcolepsy know of other family members with similar symptoms. Most people with the condition have no family members with narcolepsy.
No.
Although Polio is a contagious disease, it is not hereditary or genetic.
Narcolepsy
yes, but they can be prevented by practicing a healthy lifestyle.
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Yes.