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A Japanese Case of Primary Ciliary Dyskinesia with DNAH5 Mutations
A 33-year-old woman presented with a productive cough from childhood. She had suffered from repeated bacterial pneumonia. Her clinical and imaging findings revealed chronic sinusitis, bronchiectasis and situs inversus. We suspected primary ciliary dyskinesia (PCD) and performed a bronchial mucosal b...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Intern Med |
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| Κύριοι συγγραφείς: | , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
The Japanese Society of Internal Medicine
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6746640/ https://ncbi.nlm.nih.gov/pubmed/31118369 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2169/internalmedicine.1961-18 |
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