This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages without signing in

Hyperlipidaemia (type II)

Authoring team

This is the most common primary hyperlipidaemia. Polygenic hypercholesterolaemia is, like height, the consequence of several genes together with acquired, largely nutritional factors.

Polygenic hypercholesterolaemia causes a similar pattern of hypercholesterolaemia to that seen in familial hypercholesterolaemia (FH) (but milder than FH with cholesterol levels >6.5 mmol/L. It is characterised by increased levels of LDL-cholesterol (> 4.0 mmol/L). Triglyceride levels are < 2.3 mmol/L.

There is an increased risk of coronary heart disease but xanthomata do not develop.

Note in familial hypercholesterolaemia characteristically total cholesterol is > 7.5mmol/L, LDL-cholesterol is > 5.0 mmol/L and triglyceride is < 2.3 mmol/L.


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.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.