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Cytoplasmic “ciliary inclusions” in Isolation Are Not Sufficient for the Diagnosis of Primary Ciliary Dyskinesia
BACKGROUND: The diagnosis of primary ciliary dyskinesia (PCD) is difficult, and requires a combination of clinical features, nasal nitric oxide testing, cilia ultrastructural analysis by electron microscopy (EM), and genetics. A recently described cytoplasmic ultrastructural change termed “ciliary i...
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| Veröffentlicht in: | Pediatr Pulmonol |
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| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7068840/ https://ncbi.nlm.nih.gov/pubmed/31549486 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ppul.24528 |
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