Mechanobiology in the Comorbidities of Ehlers Danlos Syndrome

Ehlers-Danlos Syndromes (EDSs) are a group of connective tissue disorders, characterized by skin stretchability, joint hypermobility and instability. Mechanically, various tissues from EDS patients exhibit lowered elastic modulus and lowered ultimate strength. This change in mechanics has been associated with EDS symptoms. However, recent evidence points toward a possibility that the comorbidities of EDS could be also associated with reduced tissue stiffness. In this review, we focus on mast cell activation syndrome and impaired wound healing, comorbidities associated with the classical type (cEDS) and the hypermobile type (hEDS), respectively, and discuss potential mechanobiological pathways involved in the comorbidities.

Automated summary

Ehlers-Danlos Syndromes (EDS) are a group of connective tissue disorders characterized by skin stretchability, joint hypermobility, and instability, possibly associated with reduced tissue stiffness. Comorbidities include mast cell activation syndrome and impaired wound healing, and potential mechanobiological mechanisms need further investigation.