Page last updated: 2024-10-26

eperisone and Hyperargininemia

eperisone has been researched along with Hyperargininemia in 1 studies

eperisone : A racemate that is an equimolar mixture of (R)- and (S)-eperisone. It is used (as the hydrochloride salt) as a muscle relaxant for the symptomatic treatment of muscle spasm and spasticity.
1-(4-ethylphenyl)-2-methyl-3-(piperidin-1-yl)propan-1-one : An aromatic ketone that is N-propylpiperidine in which a hydrogen at positon 2 of the propyl group is replaced by a p-ethylbenzoyl group.

Hyperargininemia: A rare autosomal recessive disorder of the urea cycle. It is caused by a deficiency of the hepatic enzyme ARGINASE. Arginine is elevated in the blood and cerebrospinal fluid, and periodic HYPERAMMONEMIA may occur. Disease onset is usually in infancy or early childhood. Clinical manifestations include seizures, microcephaly, progressive mental impairment, hypotonia, ataxia, spastic diplegia, and quadriparesis. (From Hum Genet 1993 Mar;91(1):1-5; Menkes, Textbook of Child Neurology, 5th ed, p51)

Research Excerpts

ExcerptRelevanceReference
"Arginineemia, also known as arginase deficiency, is a rare autosomal recessive metabolic disease."1.56A novel compound heterozygous mutation in the arginase-1 gene identified in a Chinese patient with argininemia: A case report. ( Cao, L; Cui, D; Hu, L; Jin, L; Liu, Y, 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
Cui, D1
Liu, Y1
Jin, L1
Hu, L1
Cao, L1

Other Studies

1 other study available for eperisone and Hyperargininemia

ArticleYear
A novel compound heterozygous mutation in the arginase-1 gene identified in a Chinese patient with argininemia: A case report.
    Medicine, 2020, Aug-07, Volume: 99, Issue:32

    Topics: Arginase; Baclofen; Botulinum Toxins; Cerebral Palsy; Child; China; Diet, Protein-Restricted; Humans

2020