Familial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance
β Scribed by T. Perniola; L. Margari; M.G. de Iaco; A. Presicci; P. Ventura; E. Ferrannini; G. Illiceto
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 177 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0885-3185
- DOI
- 10.1002/mds.1117
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β¦ Synopsis
Abstract
Only few sporadic and familial cases of paroxysmal exerciseβinduced 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 longβlasting 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 ageβdependent 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. Β© 2001 Movement Disorder Society.
π SIMILAR VOLUMES
comprises mental retardation, craniosynostosis, congenital microcephaly, growth failure, glaucoma, congenital heart anomalies, and gastrointestinal defects, e.g., diaphragmatic hernia. It was first described by Lowry and Maclean [1977] in a female patient with Crouzon-like facial anomalies and other