rss
Heart 82:621-624 doi:10.1136/hrt.82.5.621
  • Paper

A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy

Table 1

Clinical details of family B

Patient Age (years) ECG LVWT on echo (mm) LA on
echo (mm)
Diastolic abnormalities
1 43 AF 13 40 +
2 56 AF 11 59 +
3 49 SR/Dom RV1/repolarisation  abnormalities 13 42
4 24 AF 13 71 +
5 27 SR/Dom RV1/repolarisation  abnormalities 11 45 +
  • AF, atrial fibrillation; Dom RV1, dominant R wave in lead V1; LA, left atrium; LVWT, left ventricular wall thickness; SR, sinus rhythm; +, present; −, absent.

This Article

Latest from Education in Heart

Latest from Education in Heart

Register for free content


Free sample
This recent issue is free to all users to allow everyone the opportunity to see the full scope and typical content of Heart.
View free sample issue >>

Free archive
The full back archive is now available for Heart. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006, back to volume 1 issue 1.
Register to access the free archive >>

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.