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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Pediatr Pulmonol
Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2019
Soggetti:
Article
Accesso online: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
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi