Résumé
We report a boy with rigidity and hyperekplexia or startle disease which began in adolescence. His symptoms completely resolved with valproic acid therapy. Two relatives have the minor form of this disorder, suggesting autosomal dominant inheritance with variable penetrance.
Langue d'origine | English |
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Pages (de-à) | 126-127 |
Nombre de pages | 2 |
Journal | Pediatric Neurology |
Volume | 5 |
Numéro de publication | 2 |
DOI | |
Statut de publication | Published - 1989 |
ASJC Scopus Subject Areas
- Pediatrics, Perinatology, and Child Health
- Neurology
- Developmental Neuroscience
- Clinical Neurology