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dc.contributor.authorColebundersa, Robert
dc.contributor.authorAbd-Elfarag, Gasim
dc.contributor.authorCarter, Jane Y.
dc.contributor.authorOloree, Peter Claver
dc.contributor.authorPuokf, Kai
dc.contributor.authorMenona, Sonia
dc.contributor.authorSiewea, Joseph Nelson Fodjo
dc.contributor.authorBhattacharyyag, Samit
dc.contributor.authorOjoke, Morrish
dc.contributor.authorLogorai, Makoy Yibi
dc.contributor.authorLakoh, Richard
dc.date.accessioned2022-02-01T20:31:55Z
dc.date.available2022-02-01T20:31:55Z
dc.date.issued2018-11
dc.identifier.citationColebunders R, Abd-Elfarag G, Carter JY, Olore PC, Puok K, Menon S, Fodjo Siewe JN, Bhattacharyya S, Ojok M, Lako R, Logora MY. Clinical characteristics of onchocerciasis-associated epilepsy in villages in Maridi County, Republic of South Sudan. Seizure. 2018 Nov;62:108-115. doi: 10.1016/j.seizure.2018.10.004. Epub 2018 Oct 5. PMID: 30340162.en_US
dc.identifier.otherhttps://doi.org/10.1016/j.seizure.2018.10.004
dc.identifier.otherPMID: 30340162
dc.identifier.urihttps://repository.amref.ac.ke/handle/123456789/564
dc.description© 2018 The Authors. Published by Elsevier Ltd on behalf of British Epilepsy Association. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).en_US
dc.description.abstractC T Purpose: To describe the clinical manifestations of persons with epilepsy (PWE) in onchocerciasis endemic villages in South Sudan. Methods: During a survey in Maridi County in May 2018, PWE were interviewed and examined in their households by a clinical o cer or medical doctor. Onchocerciasis-associated epilepsy (OAE) was de ned as 2 seizures without any obvious cause, starting between the ages of 3–18 years in previously healthy persons who had resided for at least 3 years in the onchocerciasis endemic area. Results: Seven hundred and thirty-six PWE were included in the study; 315 (42.8%) were females; median age was 18 years. A variety of seizure types were reported: generalized tonic-clonic seizures in 511 PWE (69.4%), absences in 15 (2.0%), focal motor seizures with full awareness in 7 (1.0%), focal motor seizures with impaired awareness in 25 (3.4%), brief episodes of hallucinations in 316 (43.9%) and nodding seizures in 335 (45.5%). The median age of onset of all seizures was 10 years, and 8 years for nodding seizures. PWE with nodding seizures presented with more cognitive disabilities. The diagnostic criteria for OAE were met by 414 (85.2%) of the 486 PWE with complete information. Eighty (11.0%) PWE presented with Nakalanga features. Only 378 (51.4%) PWE were taking anti-epileptic treatment. Conclusion: PWE presented with a wide spectrum of seizures. The high percentage of PWE who met the diagnostic criteria for OAE suggests that better onchocerciasis control could prevent new cases. Urgent action is needed toen_US
dc.description.sponsorshipThe European Research Council (ERC) grant number 671055, project title NSETHIOen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectOnchocerciasisen_US
dc.subjectEpilepsyen_US
dc.subjectNodding syndromeen_US
dc.subjectNakalanga syndromeen_US
dc.subjectIvermectinen_US
dc.subjectTreatmenten_US
dc.subjectMaridien_US
dc.subjectSouth Sudanen_US
dc.titleClinical Characteristics of Onchocerciasis-associated Epilepsy in Villages in Maridi County, Republic of South Sudanen_US
dc.typeArticle, Journalen_US


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