Page last updated: 2024-10-26

edrophonium and Congenital Myasthenia

edrophonium has been researched along with Congenital Myasthenia in 3 studies

Edrophonium: A rapid-onset, short-acting cholinesterase inhibitor used in cardiac arrhythmias and in the diagnosis of myasthenia gravis. It has also been used as an antidote to curare principles.
edrophonium : A quaternary ammonium ion that is N-ethyl-N,N-dimethylanilinium in which one of the meta positions is substituted by a hydroxy group. It is a reversible inhibitor of cholinesterase, with a rapid onset (30-60 seconds after injection) but a short duration of action (5-15 minutes). The chloride salt is used in myasthenia gravis both diagnostically and to distinguish between under- or over-treatment with other anticholinesterases. It has also been used for the reversal of neuromuscular blockade in anaesthesia, and for the management of poisoning due to tetrodotoxin, a neuromuscular blocking toxin found in puffer fish and other marine animals.

Research Excerpts

ExcerptRelevanceReference
"Most congenital myasthenic syndromes (CMS) have postsynaptic defects from mutations within the muscle acetylcholine receptor (AChR)."1.32Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndrome. ( Beeson, D; Brydson, M; Croxen, R; Newsom-Davis, J; Vincent, A; Webster, R, 2004)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ohkawara, B1
Cabrera-Serrano, M1
Nakata, T1
Milone, M1
Asai, N1
Ito, K1
Ito, M1
Masuda, A1
Ito, Y1
Engel, AG1
Ohno, K1
Schara, U1
Della Marina, A1
Abicht, A1
Webster, R1
Brydson, M1
Croxen, R1
Newsom-Davis, J1
Vincent, A1
Beeson, D1

Reviews

1 review available for edrophonium and Congenital Myasthenia

ArticleYear
Congenital myasthenic syndromes: current diagnostic and therapeutic approaches.
    Neuropediatrics, 2012, Volume: 43, Issue:4

    Topics: Acetylcholinesterase; Adolescent; Biopsy; Child; Cholinesterase Inhibitors; Diagnosis, Differential;

2012

Other Studies

2 other studies available for edrophonium and Congenital Myasthenia

ArticleYear
LRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific manner.
    Human molecular genetics, 2014, Apr-01, Volume: 23, Issue:7

    Topics: Adolescent; Agrin; Animals; Base Sequence; beta Catenin; Cell Line; Chlorocebus aethiops; Cholinergi

2014
Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndrome.
    Neurology, 2004, Apr-13, Volume: 62, Issue:7

    Topics: Adolescent; Amino Acid Sequence; Biopsy; Cell Line; DNA Mutational Analysis; Edrophonium; Electrodia

2004