Abstract
Electrocardiograms were recorded at baseline and regular intervals in 53 patients with myotonic dystrophy who were followed for a mean of 6.3 +/- 4.0 years. Patients with cardiac events had a significantly prolonged PR interval (p <0.001), a later age of onset of neuromuscular symptoms (p <0.05), and were older (p <0.005).
Publication types
-
Research Support, Non-U.S. Gov't
-
Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
-
Adult
-
Death, Sudden, Cardiac
-
Electrocardiography*
-
Female
-
Follow-Up Studies
-
Heart Diseases / diagnosis*
-
Heart Diseases / mortality*
-
Heart Diseases / physiopathology
-
Humans
-
Male
-
Myotonic Dystrophy / mortality
-
Myotonic Dystrophy / physiopathology*
-
Predictive Value of Tests
-
Risk Factors
-
Survival Rate
-
Time Factors