| Literature DB >> 29288080 |
Robert Colebunders1, F J Nelson Siewe2, An Hotterbeekx2.
Abstract
A high prevalence of epilepsy has been observed in onchocerciasis-endemic regions with high onchocerciasis transmission. Recent epidemiological studies suggest that Onchocerca volvulus infection is the trigger causing the seizures, which appear in previously healthy children between the ages of 3 and 18 years. Persons with onchocerciasis-associated epilepsy present with a wide spectrum of seizures, including atonic and myoclonic neck seizures; but also absences and most frequently generalized tonic-clonic seizures. Often individuals present with intellectual disabilities and psychiatric disorders and occasionally with 'Nakalanga' features such as severe stunting with delayed or absent external signs of sexual development. Onchocerciasis-associated epilepsy, because of its importance as a public health problem, is an additional reason for strengthening onchocerciasis elimination programs.Entities:
Keywords: Nakalanga syndrome; autoimmunity; epilepsy; leiomodin-1; nodding syndrome; onchocerciasis
Mesh:
Year: 2017 PMID: 29288080 DOI: 10.1016/j.pt.2017.11.009
Source DB: PubMed Journal: Trends Parasitol ISSN: 1471-4922