4Genetics
Hereditary or familial amyloidosis is a rare form that can be passed down from generation to generation. This means that having a close relative such as parents or cousins with this condition would increase the risk of developing some symptoms. Studies have found some genetic defects that can be associated with amyloid disease. TTR or transthyretin can be a major trigger. When it comes to gender, up to 65 percent of reported cases are male. The condition is also more common in people from 50 to 80 years old. Compared to other races, African-Americans are often at higher risks for hereditary amyloidosis. [4]
