Familial paroxysmal exercise‐induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance
Identifieur interne : 003030 ( Istex/Checkpoint ); précédent : 003029; suivant : 003031Familial paroxysmal exercise‐induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance
Auteurs : T. Perniola [Italie] ; L. Margari [Italie] ; M. G. De Iaco [Italie] ; A. Presicci [Italie] ; P. Ventura [Italie] ; E. Ferrannini [Italie] ; G. Illiceto [Italie]Source :
- Movement Disorders [ 0885-3185 ] ; 2001-07.
English descriptors
Abstract
Only few sporadic and familial cases of paroxysmal exercise‐induced dyskinesia (PED) have been described in literature. PED associated with familial epilepsy has been rarely reported. We describe a family in which six members in different generations were affected by a long‐lasting PED, with childhood onset in five cases. Fasting and stress were also precipitating factors. All the subjects, moreover, showed epileptic seizures during childhood and adolescence. In addition, in all cases a condition of mild mental retardation was also documented, associated in some cases, with irritable and impulsive behaviour. Clinical, neurophysiological, neuroimaging and neuropsychological findings were reported. The homogeneous recurrence of this particular clinical picture in members of three generations emphasised a common genetic basis. In our patients, PED is transmitted as an autosomal dominant trait, with age‐dependent penetrance, without evidence of genetic anticipation. The neurophysiological findings suggest a condition of hyperexcitability in the muscular and brain membrane, due to a ion channels disorder. © 2001 Movement Disorder Society.
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DOI: 10.1002/mds.1117
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PED associated with familial epilepsy has been rarely reported. We describe a family in which six members in different generations were affected by a long‐lasting PED, with childhood onset in five cases. Fasting and stress were also precipitating factors. All the subjects, moreover, showed epileptic seizures during childhood and adolescence. In addition, in all cases a condition of mild mental retardation was also documented, associated in some cases, with irritable and impulsive behaviour. Clinical, neurophysiological, neuroimaging and neuropsychological findings were reported. The homogeneous recurrence of this particular clinical picture in members of three generations emphasised a common genetic basis. In our patients, PED is transmitted as an autosomal dominant trait, with age‐dependent penetrance, without evidence of genetic anticipation. The neurophysiological findings suggest a condition of hyperexcitability in the muscular and brain membrane, due to a ion channels disorder. © 2001 Movement Disorder Society.</div></front></TEI><affiliations><list><country><li>Italie</li></country></list><tree><country name="Italie"><noRegion><name sortKey="Perniola, T" sort="Perniola, T" uniqKey="Perniola T" first="T." last="Perniola">T. Perniola</name></noRegion><name sortKey="De Iaco, M G" sort="De Iaco, M G" uniqKey="De Iaco M" first="M. G." last="De Iaco">M. G. De Iaco</name><name sortKey="Ferrannini, E" sort="Ferrannini, E" uniqKey="Ferrannini E" first="E." last="Ferrannini">E. Ferrannini</name><name sortKey="Illiceto, G" sort="Illiceto, G" uniqKey="Illiceto G" first="G." last="Illiceto">G. Illiceto</name><name sortKey="Margari, L" sort="Margari, L" uniqKey="Margari L" first="L." last="Margari">L. Margari</name><name sortKey="Presicci, A" sort="Presicci, A" uniqKey="Presicci A" first="A." last="Presicci">A. 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