Novel homozygous C3orf67 gene variant associated with primary ciliary dyskinesia in a Saudi pediatric patient: A case report

Figure 1 Family pedigree of the patient - the pedigree highlights affected individuals with a black fill, consanguinity is indicated with a double line, and genotype information is annotated.

Figure 2 Chest X-ray and computed tomography. A: Atelectatic area at the anterior right middle lobe, visible as increased opacity; B and C: Bronchiectasis in the right middle lobe with mucus plugging and segmental collapse. Shaded areas indicate disease severity.