Further associations of congenital heart disease and genetic syndromes: report of a case of tetralogy of Fallot and Fabry's disease

Pediatr Cardiol. 1999 May-Jun;20(3):236-7. doi: 10.1007/s002469900452.
No abstract available

Publication types

  • Letter

MeSH terms

  • Aorta, Thoracic / pathology
  • Diagnosis, Differential
  • Electrocardiography
  • Fabry Disease / complications*
  • Fabry Disease / diagnosis
  • Fabry Disease / enzymology
  • Glycerol Kinase / deficiency
  • Glycerol Kinase / genetics
  • Glycolipids / metabolism
  • Humans
  • Hydrolases / deficiency
  • Hydrolases / genetics
  • Magnetic Resonance Imaging
  • Mutation
  • Sex Chromosome Aberrations / diagnosis
  • Sex Chromosome Aberrations / enzymology
  • Sex Chromosome Aberrations / genetics
  • Tetralogy of Fallot / complications*
  • Tetralogy of Fallot / diagnosis
  • Tetralogy of Fallot / metabolism
  • X Chromosome
  • alpha-Galactosidase / genetics

Substances

  • Glycolipids
  • Glycerol Kinase
  • Hydrolases
  • alpha-Galactosidase