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The head nodding syndrome--clinical classification and possible causes.
Andrea S Winkler1, Katrin Friedrich, Rebekka König
1Department of Neurology, University of Ulm, Ulm, Germany. drawinkler@yahoo.com.au
Epilepsia
|May 28, 2008
Summary
Head nodding syndrome, a potential new epilepsy disorder in Africa, was studied in Tanzania. Findings suggest a link between Onchocerca volvulus infection and MRI brain lesions, warranting further investigation into its causes.
Area of Science:
- Neurology
- Tropical Medicine
- Epileptology
Background:
- A seizure disorder characterized by head nodding (HN) was observed in Tanzania in the 1960s.
- A similar condition, termed "nodding disease," later emerged in Sudan.
- The classification and etiology of this seizure disorder remain unclear.
Purpose of the Study:
- To comprehensively describe the clinical features of the "HN syndrome" in southern Tanzania.
- To investigate potential causes and associated pathologies of this epilepsy disorder.
- To explore possible links to infectious agents and genetic factors.
Main Methods:
- A prospective study evaluated 62 patients with head nodding.
- Diagnostic procedures included blood and cerebrospinal fluid (CSF) analysis, electroencephalography (EEG), and magnetic resonance imaging (MRI).
- Skin and CSF polymerase chain reaction (PCR) for Onchocerca volvulus was performed.
Main Results:
- Seizures were classified as "head nodding only" or "head nodding plus."
- MRI revealed hippocampus pathologies and gliotic changes in some patients.
- Skin PCR positivity for Onchocerca volvulus correlated significantly with MRI lesions, while CSF PCR was negative.
Conclusions:
- The "HN syndrome" may represent a novel epilepsy disorder prevalent in sub-Saharan Africa.
- The association between MRI lesions and Onchocerca volvulus (detected via skin PCR) is noteworthy.
- High rates of hippocampus sclerosis and familial epilepsy suggest complex pathogenetic mechanisms requiring further study.
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