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