Hyperekplexia: Unveiling a Rare Neurological Condition With a Treatable Solution-Reference-Cited by-同舟云学术

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Hyperekplexia: Unveiling a Rare Neurological Condition With a Treatable Solution

Published:2024-06-05 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Aglave Nisha R,Sontakke Rachana A,Bokade Chandrakant,Jhunjhunwala Kush

Publisher

Springer Science and Business Media LLC

Reference15 articles.

1. Hyperexplexia: A hereditary startle syndrome;Suhren O;J Neurol Sci,1966

2. Familial congenital disorder resembling stiff-man syndrome;Klein R;Am J Dis Child,1972

3. Nose tapping test inducing a generalized flexor spasm: a hallmark of hyperexplexia;Shahar E;Acta Paediatr Scand,1991

4. Hyperekplexia in the first year of life;Koning-Tijssen MA;Mov Disord Off J Mov Disord Soc,2000

5. Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease;Rees MI;Nat Genet,2006

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