Article

Cardiac amyloidosis in a patient with Ehlers-Danlos syndrome type IV1

Author and Disclosure Information

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.


 

References

Next Article: