Startle disease or hyperekplexia: Adolescent onset and response to valproate

Joseph M. Dooley; Frederick Andermann

doi:10.1016/0887-8994(89)90041-6

Startle disease or hyperekplexia: Adolescent onset and response to valproate

Joseph M. Dooley, Frederick Andermann

Medicine

Medicine

Producción científica: Contribución a una revista › Artículo › revisión exhaustiva

39 Citas (Scopus)

Resumen

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.

Idioma original	English
Páginas (desde-hasta)	126-127
Número de páginas	2
Publicación	Pediatric Neurology
Volumen	5
N.º	2
DOI	https://doi.org/10.1016/0887-8994(89)90041-6
Estado	Published - 1989

ASJC Scopus Subject Areas

Pediatrics, Perinatology, and Child Health
Neurology
Developmental Neuroscience
Clinical Neurology

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title = "Startle disease or hyperekplexia: Adolescent onset and response to valproate",

abstract = "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.",

author = "Dooley, {Joseph M.} and Frederick Andermann",

year = "1989",

doi = "10.1016/0887-8994(89)90041-6",

language = "English",

volume = "5",

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journal = "Pediatric Neurology",

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T1 - Startle disease or hyperekplexia

T2 - Adolescent onset and response to valproate

AU - Dooley, Joseph M.

AU - Andermann, Frederick

PY - 1989

Y1 - 1989

N2 - 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.

AB - 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.

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U2 - 10.1016/0887-8994(89)90041-6

DO - 10.1016/0887-8994(89)90041-6

M3 - Article

C2 - 2496695

AN - SCOPUS:0024583109

SN - 0887-8994

VL - 5

SP - 126

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JO - Pediatric Neurology

JF - Pediatric Neurology

IS - 2

ER -

Startle disease or hyperekplexia: Adolescent onset and response to valproate

Resumen

ASJC Scopus Subject Areas

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Huella

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