This detailed 16 page guide for General Practitioners and primary care practitioners covers a wide-range of issues from diagnosis, genetic testing, ongoing care pathways and more. 

Contents include : 

• Types of Testing for Genetic Haemochromatosis (GH)
• Normal ranges for serum ferritin and transferrin saturation
• Genetic counselling
• Interpretation and management of GH
• Variants of genetic haemochromatosis
• What happens when both parents are carriers for genetic haemochromatosis?
• What happens when one parent is a carrier of genetic haemochromatosis?
• What happens when one parent has genetic haemochromatosis and the other is a carrier?
• What happens when both parents have genetic haemochromatosis?
• What happens when one parent has genetic haemochromatosis?
• How to request test

It is available for NHS General Practitioners as part of our clinician education programme. For free copies, please contact our office.