This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Go to /pro/cpd-dashboard page

This page is worth 0.05 CPD credits. CPD dashboard

Go to /account/subscription-details page

This page is worth 0.05 CPD credits. Upgrade to Pro

Diagnosis

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Haemachromatosis should be considered in patients presenting with the following

  • symptoms:
    • fatigue
    • right upper quadrant abdominal pain
    • arthralgias (typically of the second and third metacarpophalangeal joints)
    • chondrocalcinosis
    • impotence, decreased libido
    • symptoms of heart failure
    • diabetes
  • physical findings
    • an enlarged liver, particularly in the presence of cirrhosis, extrahepatic manifestations of chronic liver disease
    • testicular atrophy
    • congestive heart failure
    • skin pigmentation
    • changes of porphyria cutanea tarda (PCT)
    • arthritis (1)

Initial investigations carried out in patients with HH are:

  • transferrin saturation
    • is the proportion of the iron transport protein transferrin that is saturated with iron
    • reference range for transferrin saturation is 15-45%
    • generally increased throughout the day and higher values can be seen in non fasting state
    • values can be high in
      • people with iron loading anaemias
      • those taking iron tablets or multivitamins containing iron
      • patients with hepatitis
      • people who misuse alcohol.
  • serum ferritin
    • measures body iron stores indirectly
    • values are increased in the following conditions
      • iron overload
      • viral infections and other inflammatory conditions
      • metabolic syndrome
      • cancer
      • chronic liver disease e.g - as a result of alcohol misuse
      • patients on dialysis
      • as a result of drug toxicity.
    • upper reference value for men is about 300 µg/L while for women it is 200 µg/L
      • local reference values should be used (1,2,3)

Genetic testing should be carried out in patients with symptoms and serum iron parameters suggestive of haemachromatosis.

  • C282Y and H63D HFE mutations are commonly tested
    • in a symptomatic C282Y homozygote patient, screening of first degree relatives for the presence of the genotype may be indicated
    • negative in non HFE genetic mutations (2,3)

If the diagnosis of haemachromatosis is still uncertain (after blood analysis and genetic testing) consider

  • magnetic resonance imaging
    • provides a quantitative imaging technique for the detection of iron in the liver
  • liver biopsy
    • is an alternative if facilities for MRI is not available
    • concentration of iron deposits can be measured (2,3)

Investigations for end organ damage:

  • liver function tests
  • imaging studies
  • fasting blood glucose
  • electrocardiography
  • echocardiography (3)

Reference:

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.