Case report
Aug 2026
A Rare Presentation of X-Linked Primary Ciliary Dyskinesia Due to Xq22.3 Deletion .
The importance of genetic testing for identifying rare PCD variants, facilitating early diagnosis and informing clinical management to improve long-term outcomes is highlighted.
Yan Li, Yan Su, Hejia Li
· Neuro - endocrinology letter... · 0 citations