Page last updated: 2024-10-27

flecainide and Batten Turner Congenital Myopathy

flecainide has been researched along with Batten Turner Congenital Myopathy in 6 studies

Flecainide: A potent anti-arrhythmia agent, effective in a wide range of ventricular and atrial ARRHYTHMIAS and TACHYCARDIAS.
flecainide : A monocarboxylic acid amide obtained by formal condensation of the carboxy group of 2,5-bis(2,2,2-trifluoroethoxy)benzoic acid with the primary amino group of piperidin-2-ylmethylamine. An antiarrhythmic agent used (in the form of its acetate salt) to prevent and treat tachyarrhythmia (abnormal fast rhythm of the heart).

Research Excerpts

ExcerptRelevanceReference
"More recently, severe neonatal episodic laryngospasm (SNEL) has been described in a small number of patients."2.53Flecainide-Responsive Myotonia Permanens With SNEL Onset: A New Case and Literature Review. ( Musumeci, O; Portaro, S; Rodolico, C; Sinicropi, S; Toscano, A; Valenzise, M, 2016)
"Residue G1306 Neonatal laryngospasm and unusual distribution of myotonia, muscle hypertrophy, and weakness encourage direct search for the G1306E mutation, a hotspot for de-novo mutations."1.46Myotonia permanens with Nav1.4-G1306E displays varied phenotypes during course of life. ( Bertini, E; D'Amico, A; Jurkat-Rott, K; Lehmann-Horn, F; Lomonaco, M; Merlini, L; Nelson, KR; Philippi, H; Siciliano, G; Spaans, F, 2017)
"An unusual form of painful congenital myotonia is associated with a novel SCN4A mutation causing a valine to methionine substitution in the domain 1/S6 segment of the skeletal muscle sodium channel."1.30Functional consequences of a domain 1/S6 segment sodium channel mutation associated with painful congenital myotonia. ( Bennett, PB; George, AL; Ruben, PC; VanDeCarr, D; Wang, DW, 1999)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's5 (83.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lehmann-Horn, F1
D'Amico, A2
Bertini, E1
Lomonaco, M2
Merlini, L1
Nelson, KR1
Philippi, H1
Siciliano, G1
Spaans, F1
Jurkat-Rott, K1
Desaphy, JF3
Carbonara, R2
Costanza, T1
Conte Camerino, D2
Portaro, S1
Rodolico, C1
Sinicropi, S1
Musumeci, O1
Valenzise, M1
Toscano, A1
Modoni, A2
Roussel, J1
Imbrici, P1
Pagliarani, S1
Lucchiari, S1
Lo Monaco, M1
Camerino, DC1
Wang, DW1
VanDeCarr, D1
Ruben, PC1
George, AL1
Bennett, PB1

Reviews

1 review available for flecainide and Batten Turner Congenital Myopathy

ArticleYear
Flecainide-Responsive Myotonia Permanens With SNEL Onset: A New Case and Literature Review.
    Pediatrics, 2016, Volume: 137, Issue:4

    Topics: Child; Female; Flecainide; Humans; Hypertrophy; Laryngismus; Muscle, Skeletal; Mutation; Myotonia Co

2016

Other Studies

5 other studies available for flecainide and Batten Turner Congenital Myopathy

ArticleYear
Myotonia permanens with Nav1.4-G1306E displays varied phenotypes during course of life.
    Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2017, Volume: 36, Issue:3

    Topics: Action Potentials; Adolescent; Adult; Age Factors; Child; Child, Preschool; Dyspnea; Exercise; Femal

2017
Preclinical evaluation of marketed sodium channel blockers in a rat model of myotonia discloses promising antimyotonic drugs.
    Experimental neurology, 2014, Volume: 255

    Topics: Animals; Carbamazepine; Disease Models, Animal; Flecainide; HEK293 Cells; Humans; Mexiletine; Muscle

2014
Translational approach to address therapy in myotonia permanens due to a new SCN4A mutation.
    Neurology, 2016, May-31, Volume: 86, Issue:22

    Topics: Cell Line; Child; Diagnosis, Differential; Female; Flecainide; Humans; Mexiletine; Mutation; Myotoni

2016
Dramatic improvement of myotonia permanens with flecainide: a two-case report of a possible bench-to-bedside pharmacogenetics strategy.
    European journal of clinical pharmacology, 2013, Volume: 69, Issue:4

    Topics: Female; Flecainide; Humans; Male; Mutation; Myotonia Congenita; NAV1.4 Voltage-Gated Sodium Channel;

2013
Functional consequences of a domain 1/S6 segment sodium channel mutation associated with painful congenital myotonia.
    FEBS letters, 1999, Apr-09, Volume: 448, Issue:2-3

    Topics: Animals; Anti-Arrhythmia Agents; Cell Line; Computer Simulation; Flecainide; Ion Channel Gating; Mem

1999