Familial hypercholesterolaemia (FH) is an inherited disorder of cholesterol and lipid metabolism, caused by an alteration in a single gene. Effective treatments are available. If left untreated, FH can lead to premature cardiovascular disease (CVD). FH is one of the most common genetic conditions, affecting 1 in 250 people.

Our regional FH cascade testing service raises awareness and identifies and supports people with FH. Cascade testing refers to family genetic testing - this means that if you are diagnosed with FH, your relatives may also be offered testing. FH used to be diagnosed by blood cholesterol measurements, but we now use genetic testing to get a more accurate diagnosis. One of our specialist FH nurse will explain more about the condition and genetic testing available and draw a family tree, which can help to identify if you have relatives who are at risk of having FH.

Our service covers:

Hampshire (including Isle of Wight)
West Berkshire
Surrey Heath
Farnham

Contact us

The best time to contact us is Monday to Wednesday between 8am and 2pm. Outside of these hours please leave an answer phone message and a member of the team will get back to you.

Call us on 023 8120 6483
Email GeneticsFH@uhs.nhs.uk
Wessex clinical genetics service
G level, mailpoint 627
Princess Anne Hospital
Coxford Road
Southampton
SO16 5YA

Familial hypercholesterolaemia - useful links