Page last updated: 2024-10-30

lorazepam and Tay-Sachs Disease

lorazepam has been researched along with Tay-Sachs Disease in 1 studies

Lorazepam: A benzodiazepine used as an anti-anxiety agent with few side effects. It also has hypnotic, anticonvulsant, and considerable sedative properties and has been proposed as a preanesthetic agent.

Tay-Sachs Disease: An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry.

Research

Studies (1)

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

Authors

AuthorsStudies
Rosebush, PI1
MacQueen, GM1
Clarke, JT1
Callahan, JW1
Strasberg, PM1
Mazurek, MF1

Reviews

1 review available for lorazepam and Tay-Sachs Disease

ArticleYear
Late-onset Tay-Sachs disease presenting as catatonic schizophrenia: diagnostic and treatment issues.
    The Journal of clinical psychiatry, 1995, Volume: 56, Issue:8

    Topics: Adolescent; Age Factors; Age of Onset; Benzodiazepines; beta-N-Acetylhexosaminidases; Diagnosis, Dif

1995