2023
DOI: 10.1016/j.seizure.2023.03.024
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Case definitions for onchocerciasis-associated epilepsy and nodding syndrome: A focused review

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Cited by 23 publications
(16 citation statements)
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“…The latter has been illustrated by mathematical modelling [ 57 ], which suggests that children are at high risk of increasing microfilarial loads. Added to this, as previously described, ivermectin uptake in Mvolo was consistently lower among younger age groups, especially those aged five to ten years, who are most susceptible to developing OAE [ 8 ]. Understanding and addressing the underlying reasons for the low ivermectin uptake is therefore vital.…”
Section: Discussionsupporting
confidence: 62%
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“…The latter has been illustrated by mathematical modelling [ 57 ], which suggests that children are at high risk of increasing microfilarial loads. Added to this, as previously described, ivermectin uptake in Mvolo was consistently lower among younger age groups, especially those aged five to ten years, who are most susceptible to developing OAE [ 8 ]. Understanding and addressing the underlying reasons for the low ivermectin uptake is therefore vital.…”
Section: Discussionsupporting
confidence: 62%
“…Similarly, in 2020, 264 out of 342 individuals (77%) with probable nodding syndrome experienced other types of seizures. This co-occurrence of nodding and other seizures is denoted as nodding syndrome plus and is within the spectrum of onchocerciasis-associated epilepsy [ 8 ]. § Data were only collected from 252 individuals with probable nodding syndrome in 2020 and 248 in 2022.…”
Section: Resultsmentioning
confidence: 99%
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“…OAE presents with a wide spectrum of epileptic seizures, including generalized tonic-clonic seizures, myoclonic seizures, absence seizures and head nodding seizures (Colebunders et al 2018a). Nodding and Nakalanga syndrome are considered to be phenotypic presentations of OAE (Colebunders et al 2018a;Van Cutsem et al 2023). Nakalanga syndrome is characterized by severe growth retardation, delayed sexual development, mental impairment, facial deformation, kyphoscoliosis, and epileptic seizures (Föger et al 2017;Siewe Fodjo et al 2019).…”
Section: Introductionmentioning
confidence: 99%
“…What is crucially important at the moment is a simple diagnostic approach or tool to differentiate OAE from other forms of epilepsy. Currently this is achieved by using the proposed OAE definition [ 14 ] which requires (1) good clinical history taking, (2) using epidemiological arguments, and (3) point-of-care onchocerciasis tests like the OV16 rapid diagnostic tests (or skin snip testing when possible). One major problem in overlapping Taenia solium - and onchocerciasis-endemic regions is to differentiate OAE from epilepsy caused by neurocysticercosis (NCC).…”
mentioning
confidence: 99%