Page last updated: 2024-10-21

hydroxyindoleacetic acid and Unverricht-Lundborg Syndrome

hydroxyindoleacetic acid has been researched along with Unverricht-Lundborg Syndrome in 1 studies

(5-hydroxyindol-3-yl)acetic acid : A member of the class of indole-3-acetic acids that is indole-3-acetic acid substituted by a hydroxy group at C-5.

Unverricht-Lundborg Syndrome: An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration, DYSARTHRIA, and intention tremor. Myoclonic seizures are severe and continuous, and tend to be triggered by movement, stress, and sensory stimuli. The age of onset is between 8 and 13 years, and the condition is relatively frequent in the Baltic region, especially Finland. (From Menkes, Textbook of Child Neurology, 5th ed, pp109-110)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Vaarmann, A1
Kaasik, A1
Zharkovsky, A1

Other Studies

1 other study available for hydroxyindoleacetic acid and Unverricht-Lundborg Syndrome

ArticleYear
Altered tryptophan metabolism in the brain of cystatin B-deficient mice: a model system for progressive myoclonus epilepsy.
    Epilepsia, 2006, Volume: 47, Issue:10

    Topics: Animals; Brain; Cerebellum; Cerebral Cortex; Chromatography, High Pressure Liquid; Cystatin B; Cysta

2006