Nasal obstruction and productive cough in a 12 years old girl in Basrah, Iraq; the diagnosis of Kartagener syndrome is established.

dc.contributor.authorZiyad Tariq Malghooth
dc.contributor.authorHaider Kadhem Saeed
dc.date.accessioned2026-01-01T10:17:29Z
dc.date.issued2022-01-06
dc.description.abstractKartagener syndrome (KS) is an autosomal recessive genetic disorder characterized by ciliary dyskinesia that causes defects in the action of ciliary movement affecting the nose, paranasal sinuses, lung and others. The syndrome comprises of triad situs inversus, chronic sinusitis with some times nasal polyposis and bronchiectasis. Kartagener syndrome regarded as a subset of the primary ciliary dyskinesia which manifested early in life with frequent respiratory infections, frequent sinus infections, frequent ear infections, chronic nasal congestion and Sino nasal polyposis and male infertility
dc.formatapplication/pdf
dc.identifier.urihttps://zienjournals.com/index.php/tjms/article/view/566
dc.identifier.uri10.62480/tjms.2022.vol4.pp21-26
dc.identifier.urihttps://asianeducationindex.com/handle/123456789/59269
dc.language.isoeng
dc.publisherZien Journals
dc.relationhttps://zienjournals.com/index.php/tjms/article/view/566/453
dc.rightshttps://creativecommons.org/licenses/by-nc/4.0
dc.sourceTexas Journal of Medical Science; Vol. 4 (2022): TJMS; 21-26
dc.source2770-2936
dc.subjectKartagener syndrome
dc.subjectimmotile cilia syndrome
dc.subjectBasrah
dc.subjectbronchiectasis
dc.titleNasal obstruction and productive cough in a 12 years old girl in Basrah, Iraq; the diagnosis of Kartagener syndrome is established.
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Article

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