Llwytho...
A case of Kartagener's syndrome with combined aplasia of frontal and sphenoid sinuses and hypoplasia of maxillary and ethmoid sinuses
Kartagener's syndrome (KS), characterized by a triad of bronchiectasis, chronic sinusitis, and situs inversus, is a subset of an autosomal recessive hereditary disorder of primary ciliary dyskinesia. We report the case of a 35-year-old male who presented with a history of intermittent episodes...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | J Family Community Med |
|---|---|
| Prif Awduron: | , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Wolters Kluwer - Medknow
2021
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8213105/ https://ncbi.nlm.nih.gov/pubmed/34194278 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jfcm.JFCM_304_20 |
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