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...

詳細記述

保存先:
書誌詳細
出版年:Ann Am Thorac Soc
主要な著者: 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.
フォーマット: Artigo
言語:Inglês
出版事項: American Thoracic Society 2016
主題:
Original Research
オンライン･アクセス: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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