Literature DB >> 1654742

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

L J Ptacek1, J S Trimmer, W S Agnew, J W Roberts, J H Petajan, M Leppert.   

Abstract

Paramyotonia congenita (PC), an autosomal dominant muscle disease, shares some clinical and electrophysiological similarities with another myotonic muscle disorder, hyperkalemic periodic paralysis (HYPP). However, clinical and electrophysiologic differences allow differentiation of the two disorders. The HYPP locus was recently shown to be linked to a skeletal muscle sodium-channel gene probe. We now report that PC maps to the same locus (LOD score 4.4, theta = 0 at assumed penetrance of .95). These linkage results, coupled with physiological data demonstrating abnormal sodium-channel function in patients with PC, implicate a sodium-channel gene as an important candidate for the site of mutation responsible for PC. Furthermore, this is strong evidence for the hypothesis that PC and HYPP are allelic disorders.

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Year:  1991        PMID: 1654742      PMCID: PMC1683172     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  15 in total

1.  Primary structure and functional expression of a mammalian skeletal muscle sodium channel.

Authors:  J S Trimmer; S S Cooperman; S A Tomiko; J Y Zhou; S M Crean; M B Boyle; R G Kallen; Z H Sheng; R L Barchi; F J Sigworth
Journal:  Neuron       Date:  1989-07       Impact factor: 17.173

2.  Lack of cold sensitivity in hyperkalemic periodic paralysis.

Authors:  S H Subramony; A S Wee; S K Mishra
Journal:  Muscle Nerve       Date:  1986-10       Impact factor: 3.217

Review 3.  Myotonia.

Authors:  R L Barchi
Journal:  Neurol Clin       Date:  1988-08       Impact factor: 3.806

Review 4.  The periodic paralyses.

Authors:  J E Riggs
Journal:  Neurol Clin       Date:  1988-08       Impact factor: 3.806

5.  Potassium uptake in muscle during paramyotonic weakness.

Authors:  R T Moxley; K Ricker; W J Kingston; R Böhlen
Journal:  Neurology       Date:  1989-07       Impact factor: 9.910

6.  Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene.

Authors:  B Fontaine; T S Khurana; E P Hoffman; G A Bruns; J L Haines; J A Trofatter; M P Hanson; J Rich; H McFarlane; D M Yasek
Journal:  Science       Date:  1990-11-16       Impact factor: 47.728

7.  Abnormalities of the fast sodium current in myotonic dystrophy, recessive generalized myotonia, and adynamia episodica.

Authors:  R Rüdel; J P Ruppersberg; W Spittelmeister
Journal:  Muscle Nerve       Date:  1989-04       Impact factor: 3.217

8.  Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

Authors:  L J Ptacek; F Tyler; J S Trimmer; W S Agnew; M Leppert
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

Review 9.  AAEE minimonograph #27: differential diagnosis of myotonic syndromes.

Authors:  E W Streib
Journal:  Muscle Nerve       Date:  1987-09       Impact factor: 3.217

10.  Two cases of adynamia episodica hereditaria: in vitro investigation of muscle cell membrane and contraction parameters.

Authors:  F Lehmann-Horn; R Rüdel; K Ricker; H Lorković; R Dengler; H C Hopf
Journal:  Muscle Nerve       Date:  1983-02       Impact factor: 3.217

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  28 in total

1.  Human Na+ channel fast and slow inactivation in paramyotonia congenita mutants expressed in Xenopus laevis oocytes.

Authors:  J E Richmond; D E Featherstone; P C Ruben
Journal:  J Physiol       Date:  1997-03-15       Impact factor: 5.182

2.  Phenotypic heterogeneity and the single gene.

Authors:  G K Suthers; K E Davies
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

Review 3.  Inherited disorders of voltage-gated sodium channels.

Authors:  Alfred L George
Journal:  J Clin Invest       Date:  2005-08       Impact factor: 14.808

Review 4.  Investigation of muscle disease.

Authors:  F L Mastaglia; N G Laing
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-03       Impact factor: 10.154

5.  Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second gene.

Authors:  J Wang; J Zhou; S M Todorovic; W G Feero; F Barany; R Conwit; I Hausmanowa-Petrusewicz; A Fidzianska; K Arahata; H B Wessel
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

6.  Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels.

Authors:  S C Cannon; R H Brown; D P Corey
Journal:  Biophys J       Date:  1993-07       Impact factor: 4.033

7.  Sodium channel mutations in paramyotonia congenita exhibit similar biophysical phenotypes in vitro.

Authors:  N Yang; S Ji; M Zhou; L J Ptácek; R L Barchi; R Horn; A L George
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-20       Impact factor: 11.205

8.  Loss of Na+ channel inactivation by anemone toxin (ATX II) mimics the myotonic state in hyperkalaemic periodic paralysis.

Authors:  S C Cannon; D P Corey
Journal:  J Physiol       Date:  1993-07       Impact factor: 5.182

9.  The alpha-subunit of the skeletal muscle sodium channel is encoded proximal to Tk-1 on mouse chromosome 11.

Authors:  C Ambrose; S Cheng; B Fontaine; J H Nadeau; M MacDonald; J F Gusella
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

10.  Linkage of Thomsen disease to the T-cell-receptor beta (TCRB) locus on chromosome 7q35.

Authors:  J A Abdalla; W L Casley; H K Cousin; A J Hudson; E G Murphy; F C Cornélis; L Hashimoto; G C Ebers
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

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