Recurrent Severe Infections and Bronchiectasis in a Heterozygous CFTR Mutation Carrier: A Case Report
Cystic fibrosis (CF) is associated with impaired innate immune function, including dysfunction of circulating monocytes and macrophages, and is currently classified within group V inborn errors of immunity. Emerging evidence suggests that heterozygous CFTR variants may also contribute to immune dysregulation and in...