A hypermobility type of Ehlers-Danlos Syndrome (EDS), characterized by hyperxtensibility of the joints, recurrent joint dislocations, and the onset of OSTEOARTHRITIS in the fourth decade of life. MITRAL VALVE PROLAPSE may also be present. Skin abnormalities are less severe than in other forms of the EDS. Mutations in the COL3A1 and the TNXB genes have been identified. OMIM: 130020
Also Known As:
Benign hypermobility syndrome; Ehlers-Danlos Syndrome, Hypermobility Type; Ehlers-Danlos Syndrome, Type III