Hereditary hemochromatosis genetic testing of at-risk children: what is the appropriate age?

Martin B Delatycki1, Lawrie W Powell, Katrina J Allen

  • 1Bruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Department of Paediatrics, University of Melbourne, Victoria, Australia. martin.delatycki@ghsv.org.au

Genetic Testing
|September 4, 2004
PubMed

Insights

Genetic testing for hereditary hemochromatosis in children is debated. Evidence suggests delaying testing until late teenage years is appropriate, as iron overload is rare in early life.

Area of Science:

  • Medical Genetics
  • Pediatric Gastroenterology

Background:

  • Hereditary hemochromatosis is an inherited disorder of iron metabolism.
  • Cascade testing of at-risk offspring is recommended due to the disease's preventability.

Purpose of the Study:

  • To evaluate evidence and ethical arguments for the optimal age of genetic testing for hereditary hemochromatosis in children.
  • To address the debate surrounding early childhood versus late teenage testing.

Main Methods:

  • Comprehensive literature search on iron overload in children, disease onset, and screening recommendations.
  • Analysis of objective evidence and ethical considerations for different testing ages.

Main Results:

  • Iron overload is infrequent in C282Y homozygous children during the first two decades of life.
  • Significant morbidity associated with early-onset iron overload in this population is rarely documented.

Conclusions:

  • Genetic testing for hereditary hemochromatosis can be deferred until late adolescence.
  • Testing in the cascade setting need not be offered to children until their teenage years.