Primary ciliary dyskinesia among Arabs: Where do we go from here?

Abstract:

:Primary ciliary dyskinesia (PCD), also known as immotile-cilia syndrome, is a rare genetic disease that is inherited in an autosomal recessive manner. Several studies have explored certain aspects of PCD in the Arab world, yet much is still lacking in terms of identifying the different characteristics of this disease. In this paper, we aim to briefly cover those studies published about PCD in Arab countries, as well as to provide recommendations and guidelines for future studies.

journal_name

Paediatr Respir Rev

authors

Hammoudeh S,Gadelhak W,Janahi IA

doi

10.1016/j.prrv.2018.09.002

subject

Has Abstract

pub_date

2019-02-01 00:00:00

pages

19-22

eissn

1526-0542

issn

1526-0550

pii

S1526-0542(18)30096-4

journal_volume

29

pub_type

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