the authors measured coenzyme Q10 (CoQ10) concentration in muscle biopsies from 135 patients with genetically undefined cerebellar ataxia. thirteen patients with childhood-onset ataxia and cerebellar atrophy had markedly decreased levels of CoQ10. associated symptoms included seizures, developmental delay, mental retardation, and pyramidal signs. these findings confirm the existence of an ataxic presentation of CoQ10 deficiency, which may be responsive to CoQ10 supplementation.

Lamperti, C., Naini, A., Hirano, M., De Vivo, D.c., Bertini, E., Servidei, S., et al. (2003). Cerebellar ataxia and coenzyme Q10 deficiency. NEUROLOGY, 60(7), 1206-1208 [10.1212/01.wnl.0000055089.39373.fc].

Cerebellar ataxia and coenzyme Q10 deficiency

Bertini, E.;Valeriani, M.;
2003-01-01

Abstract

the authors measured coenzyme Q10 (CoQ10) concentration in muscle biopsies from 135 patients with genetically undefined cerebellar ataxia. thirteen patients with childhood-onset ataxia and cerebellar atrophy had markedly decreased levels of CoQ10. associated symptoms included seizures, developmental delay, mental retardation, and pyramidal signs. these findings confirm the existence of an ataxic presentation of CoQ10 deficiency, which may be responsive to CoQ10 supplementation.
2003
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/39
English
Lamperti, C., Naini, A., Hirano, M., De Vivo, D.c., Bertini, E., Servidei, S., et al. (2003). Cerebellar ataxia and coenzyme Q10 deficiency. NEUROLOGY, 60(7), 1206-1208 [10.1212/01.wnl.0000055089.39373.fc].
Lamperti, C; Naini, A; Hirano, M; De Vivo, Dc; Bertini, E; Servidei, S; Valeriani, M; Lynch, D; Banwell, B; Berg, M; Dubrovsky, T; Chiriboga, C; Angel...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/369424
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