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Other researchers on this paper are Zachary Bitzer, Reema Goel, Craig Livelsberger, Neil Trushin and Jessica Yingst, Department of Public Health Sciences

Ehlers-Danlos syndrome (EDS) is a heterogeneous group of congenital connective tissue diseases caused by mutations in genes involved in the synthesis or processing of collagen fibers.1 The phenotypic manifestations of EDS vary greatly, and mild cases can go unnoticed until late in life

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