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What’s new in FH genetics?

What’s new in FH genetics?

What’s new in FH genetics?

Steve E Humphries - Marta Futema
Steve E Humphries - Marta Futema
on behalf of the Primary Care Cardiovascular Journal and the British Journal of Primary Care Nursing

$12.97 $ 12.97 $ 12.97

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Launch date: 11 Apr 2018
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Last updated: 23 Aug 2018

Reference: 187902

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Course Availability

This course is only available to trainees days after purchase. It would need to be repurchased by the trainee if not completed in the allotted time period. This course is no longer available. You will need to repurchase if you wish to take the course again.

Description

Recent advances in next generation sequencing (NGS) have reduced costs and made genetic diagnosis of familial hypercholesterolaemia (FH) quicker. This article reviews some of the technological breakthroughs in DNA testing in FH and benefits to patients and clinicians.

This CPD module was published 15 Dec 2015 for a UK audience. Although the information contained within the module is still deemed relevant and guidelines correct. Studies, products, practices and data may have been updated since date of publication and Guidelines and practices in other countries may differ from those in the UK. Readers are advised to check their local guidance and product specifications.

Objectives

On completion of this course, the learner will gain further understanding of:
Genetic diagnosis of familial hypercholesterolaemia (FH)
Steve E Humphries - Marta Futema

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Steve E Humphries - Marta Futema
on behalf of the Primary Care Cardiovascular Journal and the British Journal of Primary Care Nursing

PCCJ and BJPCN are digital platforms for primary care nurses, GPs and other healthcare professionals with a specific interest in cardiovascular disease, diabetes and related disorders.

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