A case of Kartagener syndrome with rhinolalia clausa

Kartagener syndrome is an autosomal recessive genetic ciliary disorder comprising of a classic triad of sinusitis, situs inversus and bronchiectasis. It's the one of primary ciliary dyskinesia disorders with manifestations present from childhood. Most patients of PCD have situs inversus. We pre...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Pan Afr Med J
Prif Awduron: Raoufi, Mohammed, Sator, Hicham, Lahma, Jawad, El Ayoubi, Ali, Nitassi, Sophia, Oujilal, Abdelilah, Benbouzid, Mohammed Anas, Essakalli, Leila, Elouazzani, Hanane, Rhorfi, Ismail Abderrahmane, Abid, Ahmed
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The African Field Epidemiology Network 2016
Pynciau:
Case Report
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4894734/
https://ncbi.nlm.nih.gov/pubmed/27375831
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2016.23.159.8664
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