1/4 of cases: The syndrome is inherited as a dominant trait, carried by gene fbn1, which encodes the connective protein fibrillin-1. People have a pair of fbn1 genes & because it is dominant, people who have inherited one affected fbn1 gene from either parent will have Marfan syndrome. The impact varies from mild to severe. Approximately one-quarter of the cases occur as a result of a spontaneous mutation.
Answered 2/18/2015
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