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Alternating hemiplegia in childhood: a cross-sectional study
S Nevsimalova, J Dittrich, M Havlova, A Tauberova, B Korsova, M Hajek, J Masopust, K Michalova
Language English Country Netherlands
Document type Case Reports, Clinical Trial
Grant support
IZ658
MZ0
CEP Register
- MeSH
- Child MeSH
- Adult MeSH
- Electroencephalography MeSH
- Electromyography MeSH
- Energy Metabolism physiology MeSH
- Flunarizine therapeutic use MeSH
- Hemiplegia drug therapy pathology radiography MeSH
- Tomography, Emission-Computed, Single-Photon MeSH
- Lactic Acid MeSH
- Pyruvic Acid MeSH
- Lactates blood MeSH
- Humans MeSH
- Adolescent MeSH
- Cross-Sectional Studies MeSH
- Pyruvates blood MeSH
- Evoked Potentials, Auditory physiology MeSH
- Sleep physiology MeSH
- Muscle Spasticity pathology MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Female MeSH
- Publication type
- Case Reports MeSH
- Clinical Trial MeSH
Six patients with alternating hemiplegia in childhood (AHC) were followed, some of them up to childhood. Progressive intellectual deterioration and disturbance of pyramidal, extrapyramidal and cerebellar functions were found in all of them. Multimodal evoked potential abnormalities, changes of sleep structure and HMPAO-SPECT results were correlated with increasing clinical handicap. In older patients increases in the plasma level of lactate, as well as in the lactate: pyruvate ratio, were revealed, accompanied by elevated inorganic phosphate (Pi) values on 31P MR spectroscopy. These findings support the hypothesis of a possible secondary mitochondrial deficit in AHC. However, no specific bioptic changes (muscle, skin, or buccal mucous membrane) were found, and thus the etiology of AHC remains unclear.
Department of Neurology 1st Medical Faculty Charles University Prague Czech Republic
References provided by Crossref.org
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- $a Six patients with alternating hemiplegia in childhood (AHC) were followed, some of them up to childhood. Progressive intellectual deterioration and disturbance of pyramidal, extrapyramidal and cerebellar functions were found in all of them. Multimodal evoked potential abnormalities, changes of sleep structure and HMPAO-SPECT results were correlated with increasing clinical handicap. In older patients increases in the plasma level of lactate, as well as in the lactate: pyruvate ratio, were revealed, accompanied by elevated inorganic phosphate (Pi) values on 31P MR spectroscopy. These findings support the hypothesis of a possible secondary mitochondrial deficit in AHC. However, no specific bioptic changes (muscle, skin, or buccal mucous membrane) were found, and thus the etiology of AHC remains unclear.
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