Literature DB >> 988769

Voluntary muscle involvement in hypertrophic cardiomyopathy. A study of eleven patients.

E R Smith, L P Heffernan, V E Sangalang, L M Vaughan, C S Flemington.   

Abstract

Hypertrophic cardiomyopathy is generally considered to be a primary disease of cardiac muscle, although several clinical observations suggest that the pathologic process might be more diffuse. To further examine this possibility, electromyography and voluntary muscle biopsies were done on 11 patients with hypertrophic cardiomyopathy. In 10 of 10 patients electromyography showed reductions in mean potential amplitude and duration, with an increased incidence of short-duration polyphasic deflections (findings traditionally accepted as indicative of a myopathic process). Light and electron microscopic studies of the biopsy material showed abnormalities in eight of 11 patients: four had central core or target fibers, or both, and two of these, plus four others, had subsarcolemmal mitochondrial proliferation with or without abnormal ultrastructure. These findings indicate that hypertrophic cardiomyopathy is only one aspect of a larger disease spectrum, with abnormalities in both voluntary and cardiac muscle.

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 988769     DOI: 10.7326/0003-4819-85-5-566

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  7 in total

1.  Cardiac involvement in Friedreich's ataxia.

Authors: 
Journal:  Br Med J       Date:  1978-02-04

2.  Abnormal skeletal muscle bioenergetics in familial hypertrophic cardiomyopathy.

Authors:  C H Thompson; G J Kemp; D J Taylor; M Conway; B Rajagopalan; A O'Donoghue; P Styles; W J McKenna; G K Radda
Journal:  Heart       Date:  1997-08       Impact factor: 5.994

3.  Mice expressing mutant myosin heavy chains are a model for familial hypertrophic cardiomyopathy.

Authors:  K L Vikstrom; S M Factor; L A Leinwand
Journal:  Mol Med       Date:  1996-09       Impact factor: 6.354

4.  Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy.

Authors:  P J Lamont; B Udd; F L Mastaglia; M de Visser; P Hedera; T Voit; L R Bridges; V Fabian; A Rozemuller; N G Laing
Journal:  J Neurol Neurosurg Psychiatry       Date:  2005-08-15       Impact factor: 10.154

5.  Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.

Authors:  L Fananapazir; M C Dalakas; F Cyran; G Cohn; N D Epstein
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-01       Impact factor: 11.205

6.  Restrictive and hypertrophic cardiomyopathies in Noonan syndrome: the overlap syndromes.

Authors:  P T Wilmshurst; D Katritsis
Journal:  Heart       Date:  1996-01       Impact factor: 5.994

7.  Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Cardiac Muscle Regulation.

Authors:  Tiago Veltri; Maicon Landim-Vieira; Michelle S Parvatiyar; David Gonzalez-Martinez; Karissa M Dieseldorff Jones; Clara A Michell; David Dweck; Andrew P Landstrom; P Bryant Chase; Jose R Pinto
Journal:  Front Physiol       Date:  2017-04-20       Impact factor: 4.566

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.