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trihexyphenidyl and Ataxia Telangiectasia

trihexyphenidyl has been researched along with Ataxia Telangiectasia in 1 studies

Trihexyphenidyl: One of the centrally acting MUSCARINIC ANTAGONISTS used for treatment of PARKINSONIAN DISORDERS and drug-induced extrapyramidal movement disorders and as an antispasmodic.

Ataxia Telangiectasia: An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23).

Research Excerpts

ExcerptRelevanceReference
"Severe dystonia was presented in late stage of this disease."5.56Trihexyphenidyl for treatment of dystonia in ataxia telangiectasia: a case report. ( Jia, Y; Li, M; Qi, X; Wang, S; Wang, Y; Zhang, L, 2020)
"Severe dystonia was presented in late stage of this disease."1.56Trihexyphenidyl for treatment of dystonia in ataxia telangiectasia: a case report. ( Jia, Y; Li, M; Qi, X; Wang, S; Wang, Y; Zhang, L, 2020)

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

Authors

AuthorsStudies
Zhang, L1
Jia, Y1
Qi, X1
Li, M1
Wang, S1
Wang, Y1

Other Studies

1 other study available for trihexyphenidyl and Ataxia Telangiectasia

ArticleYear
Trihexyphenidyl for treatment of dystonia in ataxia telangiectasia: a case report.
    Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2020, Volume: 36, Issue:4

    Topics: Ataxia Telangiectasia; Child; Dystonia; Dystonic Disorders; Humans; Male; Mutation; Phenotype; Trihe

2020