ABSTRACT
A patient with typical clinical features of Ehlers- Danlos syndrome Type IV was found to have systemic amyloidosis that was proved by cardiac biopsy. The various types and subtypes of Ehlers-Danlos syndrome are reviewed, along with the associated cardiac anomalies.
- Received November 1985.
- Accepted February 1986.
- Copyright © 1986 The Cleveland Clinic Foundation. All Rights Reserved.