BACKGROUND To assess the risk of psychiatric disorders in Ehlers-Danlos syndrome (EDS) and hypermobility syndrome. METHODS Nationwide population-based matched cohort study. EDS, hypermobility syndrome and psychiatric disorders were identified through Swedish national registries. Individuals with EDS (n = 1,771) were matched with comparison individuals (n = 17,710). Further, siblings to indivi...

Joint hypermobility is the defining feature of various inherited connective tissue disorders such as Marfan syndrome and various types of Ehlers-Danlos syndrome and these will generally be the first conditions to be considered by geneticists and pediatricians in the differential diagnosis of a patient presenting with such findings. However, several congenital and adult-onset inherited myopathie...

Introduction The Joint Hypermobility Syndrome (JHS) is a multi-system inherited connective tissue disorder caused by defective fibrous tissue matrix proteins such as collagen. Joint hypermobility has been occurred more frequently in children, with diminishing occurrence as age increases in population studies. The prevalence of hypermobility in children has been reported to be between 2.3 and 30...

PURPOSE To describe hypermobility, balance, pain, activity, and participation in children with hypermobility and compare these characteristics with those of a control group. METHOD Twenty children aged 8 to 16 years with hypermobility syndrome (HMS) or Ehlers-Danlos syndrome and a control group of 24 children of the same age participated in the study. Hypermobility was assessed according to t...

background: the purpose of the present study was to examine the reliability of scapular kinematic measurements using motion analysis system in subjects with and without general hypermobility syndrome. methods: a methodological study was designed to assess the reliability of scapular movement measurement in two groups of females with and without general hypermobility syndrome. upward rotation, s...

Methods Sixty-three children with benign joint hypermobility syndrome were included in case group and 63 without any rheumatologic disease were placed in control group. We used Carter-Wilkinson and Beighton criteria for diagnosing of benign joint hypermobility syndrome. MVP was evaluated by echocardiography in both groups. The mitral leaflet displacement >2 mm considered as cut off for diagnosi...

There are intimate interrelations between various elements of connective tissue, viz. collagen, elastin, and glycoproteins. It is not unexpected that Marfan and Ehlers-Danlos syndromes share common features. The condition is labelled as Marfanoid hypermobility syndrome. In the patient described here, the Marfanoid hypermobility syndrome was associated with coarctation of the aorta which was cor...

Joint hypermobility syndrome (JHS) is a hereditary disorder of connective tissue recently considered the one and the same as the Ehlers-Danlos Syndrome Hypermobility Type (EDS-HT). The JHS/EDS-HT is mainly characterized by joint hypermobility, chronic pain and a variable skin involvement. Clinical manifestations expressed by patients are multiple and varied. The rehabilitative approach may play...

Joint Hypermobility Syndrome (JHS) and Hypermobility Syndrome (HMS) are old names for a condition now called hypermobile Ehlers-Danlos Syndrome, or hEDS. hEDS is a condition in which people have pain as a result of joints that are too flexible, as well as other symptoms. Being hypermobile can be an advantage in some occupations, such as dance and music. However, people with hEDS are vulnerable ...