Kartagener's Syndrome with Seizures: A Rare Case Report
International Journal of Science and Research (IJSR)

International Journal of Science and Research (IJSR)
Call for Papers | Fully Refereed | Open Access | Double Blind Peer Reviewed

ISSN: 2319-7064


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Research Paper | Neuroscience | India | Volume 11 Issue 6, June 2022 | Popularity: 4.5 / 10


     

Kartagener's Syndrome with Seizures: A Rare Case Report

Deepika Sagar, Dheeraj Kumar Soni


Abstract: Primary Ciliary Dyskinesia (PCD) is a genetic disorder with an autosomal recessive mode of inheritance. It is caused by a defect in the structure of cilia, due to which ciliary movement, and consequently, its function, are impaired. Sinusitis, nasal polyposis, and otitis media with effusion are commonly seen among patients. Seizures are rare in such patients. We are presenting a rare case report of a patient with kartagener's syndrome who presented with seizure.


Keywords: Karatgner syndrome, seizure, sinus thrombosis


Edition: Volume 11 Issue 6, June 2022


Pages: 1681 - 1682


DOI: https://www.doi.org/10.21275/SR22621213357



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Deepika Sagar, Dheeraj Kumar Soni, "Kartagener's Syndrome with Seizures: A Rare Case Report", International Journal of Science and Research (IJSR), Volume 11 Issue 6, June 2022, pp. 1681-1682, https://www.ijsr.net/getabstract.php?paperid=SR22621213357, DOI: https://www.doi.org/10.21275/SR22621213357

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