Aby,Ehlers-Danlos syndrome has several variant types, and each can have varying degrees of expression. The common feature of E-D syndrome is joint hyper extensibility (double-jointedness) hyperstretchable skin with preservation of elasticity (skin stretches more than usual, but mostly snaps back to normal dimension), tendency to stretchmark formation, and potential for wound-healing delay or scar stretch in some patients. I prefer to use an axillary approach in my patients with Ehlers-Danlos syndrome. as that places the incisions remote to the position of the implants, and thus the implants place no tension on the healing incisions, even if there is a healing delay. I have not actually seen wound healing problems in the patients I have with Ehlers Danlos, but I have seen undiagnosed Ehlers-Danlos lead to failure of a sternal repositioning for pectus excavatum (Ravitch procedure) which had to be salvaged by subsequent placement of a Nuss bar for stability. There may be an added risk of implant bottoming-out with Ehlers-Danlos so any augmentation should be done by a technique that preserves the lower pectoralis muscle origins on the lower ribs, as those muscles provide lasting internal support for implants. I would also recommend against use of large implants that stress internal support, as that may aggravate the tendency to loss of support, as well. I hope that this helps. Information regarding axillary augmentation approach with internal muscle support preservation is found at the link that follows.