Primary ciliary dyskinesia among Arabs: Where do we go from here?
| Autor: | Ibrahim A. Janahi, Wessam Gadelhak, Samer Hammoudeh |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
Pulmonary and Respiratory Medicine
medicine.medical_specialty Yemen Future studies Saudi Arabia United Arab Emirates Disease Consanguinity Middle East 03 medical and health sciences 0302 clinical medicine otorhinolaryngologic diseases Humans Medicine 030212 general & internal medicine Qatar Primary ciliary dyskinesia Bronchiectasis Kartagener Syndrome business.industry Arab World Research medicine.disease Dermatology Arabs Kuwait 030228 respiratory system Practice Guidelines as Topic Pediatrics Perinatology and Child Health business Ciliary Motility Disorders |
| Zdroj: | Paediatric Respiratory Reviews. 29:19-22 |
| ISSN: | 1526-0542 |
| DOI: | 10.1016/j.prrv.2018.09.002 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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