Primary ciliary dyskinesia in Japan: systematic review and meta-analysis

Primary ciliary dyskinesia in Japan: systematic review and meta-analysis

Abstract Background Primary ciliary dyskinesia (PCD) is a rare genetic disorder. Although the genetic tests and new diagnostic algorithms have recently been recommended, clinical signs and electron microscope (EM) findings have historically been the mainstays of diagnosis in Asia. To characterize PC...

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Bibliographic Details
Main Authors: Atsushi Inaba, Masanori Furuhata, Kozo Morimoto, Mahbubur Rahman, Osamu Takahashi, Minako Hijikata, Michael R. Knowles, Naoto Keicho
Format: Article
Language:English
Published: BMC 2019-07-01
Series:BMC Pulmonary Medicine
Subjects:
Systematic review
Meta-analysis
Primary ciliary dyskinesia
Immotile cilia syndrome
Kartagener syndrome
Electron microscopy
Online Access:http://link.springer.com/article/10.1186/s12890-019-0897-4

Internet

http://link.springer.com/article/10.1186/s12890-019-0897-4

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