Familial cardiomyopathy

Cardiology. 1976;61(2):122-30. doi: 10.1159/000169753.

Abstract

Over three generations, several members of a family suffered from cardiomyopathy exhibiting, primarily, rhythm and conduction disturbances and, eventually, congestive heart failure. Certain serum enzymes (SGOT, SGPT, LDH) were elevated. The clinical examination indicated a progressive deterioration with increasing age of the patients, a more serious course in the male members of the family, and the frequent association of mental retardation.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Alanine Transaminase / blood
  • Arrhythmias, Cardiac / enzymology
  • Arrhythmias, Cardiac / genetics
  • Aspartate Aminotransferases / blood
  • Cardiomyopathies / enzymology
  • Cardiomyopathies / genetics*
  • Female
  • Heart Failure / enzymology
  • Heart Failure / genetics
  • Humans
  • L-Lactate Dehydrogenase / blood
  • Male
  • Middle Aged
  • Pedigree
  • Sex Factors

Substances

  • L-Lactate Dehydrogenase
  • Aspartate Aminotransferases
  • Alanine Transaminase