Page last updated: 2024-10-21

phenytoin and Unverricht-Lundborg Syndrome

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

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's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Canafoglia, L1
Ferlazzo, E1
Michelucci, R1
Striano, P1
Magaudda, A1
Gambardella, A1
Pasini, E1
Belcastro, V1
Riguzzi, P1
Fanella, M1
Granata, T1
Beccaria, F1
Trentini, C1
Bianchi, A1
Aguglia, U1
Panzica, F1
Franceschetti, S1

Other Studies

1 other study available for phenytoin and Unverricht-Lundborg Syndrome

ArticleYear
Variable course of Unverricht-Lundborg disease: Early prognostic factors.
    Neurology, 2017, Oct-17, Volume: 89, Issue:16

    Topics: Adolescent; Adult; Age of Onset; Analysis of Variance; Anticonvulsants; Cathepsin B; Electroencephal

2017