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How are the cause and onset of symptoms of huntingtons disease different from of PKU and Tay-Sachs disease?
Typcially, onset of symptoms with HD is from the mid 30-s to 40's.
How are the cause and onset of symptoms of Huntington's disease different from those of PKU and Tay Sachs disease?
Typcially, onset of symptoms with HD is from the mid 30-s to 40's.
What are the symptoms of the adult form of Alexander disease?
Symptoms that mimic multiple sclerosis , or may display symptoms similar to the juvenile form of the disease, except with later onset and slower progression.
The time between exposure to a disease causing bacteria or virus and onset of symptoms is called the?
Incubation
What is the prognosis for Binswanger disease?
Once symptoms become visible (manifest), persons with Binswanger disease often die within five years of the onset of the disease.
Why does Huntington's disease continue to survive throughout generations?
Onset of symptoms is later in life, after people have already had children.
The average time span between the initial HIV infection and the onset of disease symptoms in untreated people is?
The average time span between the initial HIV infection and the onset of disease symptoms in untreated people is 8 to 10 years but that can vary greatly. Some people never progress.
Which stage of infection is the period of time between the invasion of the infectious agent into the body and the onset of symptoms of the particular disease?
incubation
What symptoms of Canavan disease begin early?
The onset of symptoms, such as a lack of head control and poor muscle tone, usually begins by two to three months of age
What is the prognosis for Leigh disease?
Soon after the onset of symptoms, the progression of Leigh disease is unrelentingly rapid. Death usually occurs from respiratory failure within two years following the initial symptoms, and usually by age six.
What is the prognosis for Alzheimer disease?
The Alzheimer Disease Association claims that the time from the onset of clinical symptoms to death can range from three to 20 years, with an average duration of eight years.
How is it possible for huntington's chorea disease patients to be unaware of the disease and pass it onto next generation?
It is very possible. The onset of symptoms is usually later in life, after a person will have had children.
