Literature DB >> 117777

[Familial cardiomyopathy: a study of two families with myocardial and skeletal muscle biopsies].

A Sacrez, A Porte, A Batzenschlager, T De Barsy, F Wolff, D Grison, L Stoeckel, P Ferrière.   

Abstract

Cardiomyopathy was diagnosed in several members of two families. This familial cardiomyopathy showed symmetrical or asymmetrical hypertrophy of the ventricular walls with or without obstruction to the left ventricular outflow tract. Certain forms were asymptomatic and were revealed by the family history and echocardiography. Myocardial and intercostal muscle biopsy was performed for a biochemical and ultrastructural analysis. Different myocardial features were observed in the two families: a large increase in the glycogen deposits in the one, without clinical signs of a glycogen storage disease, and intracellular deposits of a filamentous protein substance in the other.

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Year:  1979        PMID: 117777

Source DB:  PubMed          Journal:  Arch Mal Coeur Vaiss        ISSN: 0003-9683


  2 in total

1.  Unusual familial cardiomyopathy with storage of intermediate filaments in the cardiac muscular cells.

Authors:  A Porte; M E Stoeckel; A Sacrez; A Batzenschlager
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1980

2.  Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study.

Authors:  E Bertini; C Bosman; E Ricci; S Servidei; R Boldrini; M Sabatelli; G Salviati
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

  2 in total

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