In most cases, HAE is caused by the mutation of a gene that is responsible for producing one of the proteins in the body's immune system. Because the disease is hereditary, a typical patient with HAE often has several family members with the condition.
However, the absence of family history doesn't rule out the diagnosis of HAE. Some newly diagnosed patients have had a spontaneous mutation of the C1-inhibitor gene - in other words, the mutation can happen even when there is no family history of HAE.
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