Show Summary Details
Page of

Hypertrophic cardiomyopathy 

Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy

M Barnard

and B Martin

Page of

PRINTED FROM OXFORD MEDICINE ONLINE ( © Oxford University Press, 2020. All Rights Reserved. Under the terms of the licence agreement, an individual user may print out a PDF of a single chapter of a title in Oxford Medicine Online for personal use (for details see Privacy Policy and Legal Notice).

date: 07 August 2020

Pathology 494

Therapeutic options 496

Haemodynamic goals 497

Anaesthetic plan and adverse haemodynamics 498

TOE essentials 500

Practice points 502

Further reading 503

Clinical prevalence estimated at 1 in 500.

Mendelian autosomal dominant trait.

Ten gene defects – encoding for sarcomere proteins.


Access to the complete content on Oxford Medicine Online requires a subscription or purchase. Public users are able to search the site and view the abstracts for each book and chapter without a subscription.

Please subscribe or login to access full text content.

If you have purchased a print title that contains an access token, please see the token for information about how to register your code.

For questions on access or troubleshooting, please check our FAQs, and if you can't find the answer there, please contact us.