Intrafamilial variability of noncompaction of the ventricular myocardium

Am Heart J. 2006 May;151(5):1012.e7-14. doi: 10.1016/j.ahj.2006.01.021.

Abstract

Background: Noncompaction of the ventricular myocardium (NVM) is a relatively uncommon form of cardiomyopathy characterized by a highly trabeculated myocardium. This report describes the clinical and genetic evaluation of a 3-generation kindred.

Methods: Family members were initially evaluated by 2-dimensional echocardiography. Most family members with signs of NVM were further evaluated by magnetic resonance imaging. Genetic analyses included mutational screening of the taffazin (TAZ) and alpha-dystrobrevin (DTNA) genes.

Results: Eight family members had signs of NVM. Considerable interindividual variation was noted in terms of spatial distribution and severity of affected regions and ventricular dysfunction. Depending on which of 2 previously proposed quantitative diagnostic criteria were used and where ventricular myocardial measurements were taken, between 4 and 7 of these individuals had findings that were considered diagnostic. Magnetic resonance imaging served as a useful adjunct for confirming or establishing diagnoses in all 8 individuals. No mutation was found in TAZ or DTNA.

Conclusions: This kindred demonstrates the remarkably wide phenotypic spectrum that can be seen in familial cases of NVM, ranging from prenatal/neonatal lethality to a complete lack of symptoms. The fact that all 8 affected individuals either have shown improvement in ventricular function or symptoms during childhood or have been asymptomatic indicates that NVM can have a relatively benign course. The degree and nature of cardiac involvement are also quite varied, and there is a weak correlation with ventricular function and symptoms. Evaluation of families with NVM requires careful assessment that uses a combination of imaging techniques and diagnostic criteria.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Cardiomyopathies / complications
  • Cardiomyopathies / diagnosis*
  • Cardiomyopathies / embryology
  • Cardiomyopathies / genetics*
  • Echocardiography*
  • Electrocardiography
  • Female
  • Genetic Variation*
  • Heart Ventricles
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Middle Aged
  • Pedigree
  • Phenotype
  • Ultrasonography, Prenatal
  • Ventricular Dysfunction / etiology
  • Ventricular Dysfunction / physiopathology