In this work it is observed the disease which is insufficiently explored in the world and absolutely unstudied in our country — Hypermobile Syndrome. It is known that it is a hereditary disease, but the questions as for the type of inheritance remain open at present; there is no scientific information in the literature about genetic markers. With the aim to find out the genetic marker of the risk of HMS development the investigation of the system of tissue hystocompatibility based on the results of HLA- and DR-typing for the first time was conducted in the Odessa State Medical University. The acknowleged results don’t have national analogs because this problem has not been studied in our country and in foreign literature the works on this problem have not been found.
