Friedreich's Ataxia With Acute Cardiomyopathy
- 1 April 1980
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Pediatrics & Adolescent Medicine
- Vol. 134 (4) , 390-393
- https://doi.org/10.1001/archpedi.1980.04490010044015
Abstract
• Friedreich's ataxia (FA) is a progressive, spinocerebellar degenerative disease. Onset is generally in the second decade of life, occurring as a neurologic degenerative process. Most, if not all, patients have an associated cardiomyopathy, which is frequently the cause of death. We studied two siblings who had FA with acute cardiomyopathy at 3 and 5 years of age, respectively, and in whom the classic nervous system signs developed, only later. The diagnosis of FA should be considered in patients of any age who have unexplained cardiomyopathy. (Am J Dis Child134:390-393, 1980)This publication has 2 references indexed in Scilit:
- Hypertrophic cardiomyopathy: The heart disease of Friedreich's ataxiaAmerican Heart Journal, 1977
- Hypertrophic Subaortic Stenosis Occurring in a Patient with Friedreich??s AtaxiaThe Lancet Healthy Longevity, 1970