Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge

Manal Albalawi; Abdullah Al-Shamrani; Ahmed Sarar Mohamed; Sarar Mohamed

doi:10.12659/AJCR.942444

24 March 2024 : Case report Saudi Arabia

Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge

Unknown etiology, Unusual clinical course, Challenging differential diagnosis, Rare coexistence of disease or pathology

Manal Albalawi^1BEG*, Abdullah Al-Shamrani^23ABD, Ahmed Sarar Mohamed^4EF, Sarar Mohamed^23ACDF

DOI: 10.12659/AJCR.942444

Am J Case Rep 2024; 25:e942444

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Introduction Case Report Discussion Conclusions References:

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Figure 2. Chest X-ray with marked hyperinflation and marked radiolucency in the left upper zone, with no vascular vessels suggestive of a localized cyst (black arrow). Furthermore, multiple cavitations in the right upper and middle zones were observed.

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Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge

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