[Skip to Navigation]
[Skip to Navigation Landing]
October 1974

Multiple Forms of the Ehlers-Danlos Syndrome

Author Affiliations

Department of Medicine Johns Hopkins Hospital Baltimore, MD 21205

Arch Surg. 1974;109(4):475-476. doi:10.1001/archsurg.1974.01360040001001

This article is only available in the PDF format. Download the PDF to view the article, as well as its associated figures and tables.


The Ehlers-Danlos syndrome (or, as we shall attempt to emphasize here, the Ehlers-Danlos syndromes) is characterized mainly by changes in the joints and in the skin. The joint change is hyperextensibility, ie, loose-jointedness. The skin change is classically excessive stretchability, excessive bruisability, and excessive fragility.

In the last ten years or so, many genetic disorders that in the past were considered to be a single entity have, on close scrutiny, been found to be a collection of two or more fundamentally distinct disorders. The Ehlers-Danlos syndrome is no exception to this experience. Today at least seven seemingly distinct forms of the Ehlers-Danlos syndrome can be recognized (Table), and this may well not exhaust the heterogeneity within this group.

As with other categories of genetic disease, clinical features, genetic factors, and biochemical approaches have been used to distinguish the various forms. Of the three approaches, the biochemical one is the most

First Page Preview View Large
First page PDF preview
First page PDF preview