Bronchiectasis in a child with a homozygous DCDC2 gene mutation: A case report
Abstract
mutations and respiratory involvement. Early recognition of this association might support timely pulmonary screening and intervention to improve long-term outcomes.
Fields of Study & Subjects
Cystic Fibrosis Research Advances
Genomics and Rare Diseases
Immunodeficiency and Autoimmune Disorders
Publication details
- Journal / source
- Journal of Taibah University Medical Sciences
- Volume
- 21
- Issue
- 1
- Pages
- 159–163
- Publication date
- 1 February 2026
- Language
- EN