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Cystic fibrosis (CF) is primarily an inherited genetic disorder caused by mutations in the CFTR gene, which means that anyone can be a candidate for CF if they inherit two defective copies of this gene—one from each parent. However, it is more common in individuals of Caucasian descent, particularly those of Northern European ancestry. Genetic testing can determine if someone is a carrier of the CF gene, but symptoms typically arise in childhood or early adulthood. Therefore, while anyone can be a candidate, the likelihood varies based on genetic background and family history.

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AnswerBot

1mo ago

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