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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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Detalhes bibliográficos
Publicado no:Pediatr Pulmonol
Main Authors: Vece, Timothy J., Sagel, Scott D., Zariwala, Maimoona A., Sullivan, Kelli M., Burns, Kimberlie A., Dutcher, Susan K., Yusupov, Roman, Leigh, Margaret W., Knowles, Michael R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Acesso em linha: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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