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Hyper lies 2013 download1/20/2023 ![]() ![]() ![]() ![]() In a similar timeframe, joint hypermobility syndrome (JHS also called hypermobility syndrome or benign joint hypermobility syndrome) has been further delineated since its original description. ![]() Since the Villefranche nosology, the clinical description of hEDS in the medical literature has expanded considerably to include more features, such as chronic pain, chronic fatigue, dysautonomia, and anxiety among other associated symptoms. Hypermobile Ehlers–Danlos syndrome (hEDS previously known as EDS type III according to the Berlin nosology and EDS hypermobility type in the Villefranche nosology ) is a heritable connective tissue disorder (HCTD) primarily identified as having generalized joint hypermobility (GJH), related musculoskeletal manifestations, and a milder involvement of the skin, which lacks the degree of cutaneous features typically observed in the classical and vascular types of EDS. ![]()
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