Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents

Rationale: Primary ciliary dyskinesia (PCD), a genetically heterogeneous, recessive disorder of motile cilia, is associated with distinct clinical features. Diagnostic tests, including ultrastructural analysis of cilia, nasal nitric oxide measurements, and molecular testing for mutations in PCD gene...

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Pubblicato in:Ann Am Thorac Soc
Autori principali: Leigh, Margaret W., Ferkol, Thomas W., Davis, Stephanie D., Lee, Hye-Seung, Rosenfeld, Margaret, Dell, Sharon D., Sagel, Scott D., Milla, Carlos, Olivier, Kenneth N., Sullivan, Kelli M., Zariwala, Maimoona A., Pittman, Jessica E., Shapiro, Adam J., Carson, Johnny L., Krischer, Jeffrey, Hazucha, Milan J., Knowles, Michael R.
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Thoracic Society 2016
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Original Research
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5021075/
https://ncbi.nlm.nih.gov/pubmed/27070726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/AnnalsATS.201511-748OC
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