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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Pan Afr Med J
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The African Field Epidemiology Network 2016
Aiheet:
Case Report
Linkit: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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