30Jun 2024

CLINICAL MANIFESTATIONS AND DIAGNOSTIC CHALLENGES OF KARTAGENER SYNDROME

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Kartagener syndrome (KS) is an uncommon autosomal recessive genetic disorder characterized by the triad of bronchiectasis, chronic rhinosinusitis, and situs inversus. It is a specific phenotype within the spectrum of primary ciliary dyskinesia (PCD), a condition involving dysfunctional ciliary motility. Early diagnosis is crucial for effective management of the associated respiratory complications.

[A.El Ouali, I. Bounnite, S. Moussaoui, M. Labied, C. Mountassir, G. Lembarki, M. Sabiri and S. Lezar (2024); CLINICAL MANIFESTATIONS AND DIAGNOSTIC CHALLENGES OF KARTAGENER SYNDROME Int. J. of Adv. Res. (Jun). 909-913] (ISSN 2320-5407). www.journalijar.com

Imane bounnite
A.El Ouali, I,Bounnite, S.Moussaoui, M.Labied,C.Mountassir, G.Lembarki,M.Sabiri,S.Lezar
Morocco

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Article DOI: 10.21474/IJAR01/18954      
DOI URL: https://dx.doi.org/10.21474/IJAR01/18954

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