Genetic investigation of sinopulmonary diseases in Vietnam: seeking specific causes from non-specific symptoms
This is the first report in Vietnamese patients with non-specific upper and lower airway symptoms to identify genetic variants specific to CF and PCD, as well as another variant potentially associated with DPB. For the future management of sinopulmonary diseases or BE with unknown causes, ethnic differences based on their genetic etiology should be carefully considered.
Authors
- Naoto Keicho (ORCID: https://orcid.org/0000-0001-8232-9448)
- Kozo Morimoto (ORCID: https://orcid.org/0000-0002-8239-9275)
- Nguyen Thu Huyen (ORCID: https://orcid.org/0000-0002-5053-5682)
- Ngo Quy Chau (ORCID: https://orcid.org/0000-0002-6787-2757)
- Akiko Miyabayashi
- Phạm Thị Bích (ORCID: https://orcid.org/0000-0002-4780-3439)
- Keiko Wakabayashi
- Nguyen Thi Le Hang
- Minako Hijikata (ORCID: https://orcid.org/0000-0002-1642-6597)
- Phan Thu Phuong
- Le Cong Dinh
Institutions
- Hanoi Medical University (VN)
- Enterprise Ireland (IE)
- Japan Anti Tuberculosis Association (JP)
- Institute of Information Security (JP)
- Khanh Hoa General Hospital (VN)
- Bạch Mai Hospital (VN)
- Fukujuji Hospital (JP)
Publication Details
- Journal
- Orphanet Journal of Rare Diseases
- Published
- 2025-10-15
- DOI
- https://doi.org/10.1186/s13023-025-04031-5
- Primary Topic
- Cystic Fibrosis Research Advances
- Type
- article
- Field-Weighted Citation Impact
- 0.00