Abstract
We studied a syndrome involving a progressive atrioventricular conduction defect in three generations of a large family. Clinical findings included a slow heart rate, episodes of lightheadedness, syncope, and absence of predisposing acquired or hereditary cardiac disorders. Electrocardiography showed a prolonged atrioventricular conduction with onset usually in the 30s, loss of R waves in the right precordial leads, and arrhythmia that occurs only as a late manifestation. Progression from first-degree to complete heart block was usually slow, but occasionally a fulminant course led to sudden death within two or three years. Specific differences from other forms of conduction defects suggest that this is a new hereditary syndrome. © 1973, American Medical Association. All rights reserved.
Cite
CITATION STYLE
Lynch, H. T., Mohiuddin, S., Sketch, M. H., Krush, A. J., Carter, S., & Runco, V. (1973). Hereditary Progressive Atrioventricular Conduction Defect: A New Syndrome? JAMA: The Journal of the American Medical Association, 225(12), 1465–1470. https://doi.org/10.1001/jama.1973.03220400011003
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.