1) How does a person inherit it? Is it dominant orrecessive?
2) What are the possible genotypes of the parents? If thedisease is a chromosomal abnormality describe theabnormality.
3) How prevalent is the disease in the population ( includingstatistics)?
4) What are the chances of a person with this disease passingthe disease on to their offspring ( include possiblescenarios)?
5) How is the disease diagnosed?
6) What are the physical symptoms of the disease?
7) What is the life expectancy of someone with the disease?
8) How can he disease be treated?