Primary ciliary dyskinesia among Arabs: Where do we go from here? - 21/03/19
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.
Le texte complet de cet article est disponible en PDF.Abbreviations : CTGA, CAGS, CCDC151, DNAH, GDMCC, iPCD Cohort, LRRC6, PCD, PICADAR, RDCRN, USA, UAE, UAEGDA, wgSNP
Keywords : Primary ciliary dyskinesia, Immotile-cilia syndrome, Kartagener syndrome, Bronchiectasis, Arab, Qatar
Plan
Vol 29
P. 19-22 - février 2019 Retour au numéro
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