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Hypermobility spectrum disorder (HSD), related to earlier diagnoses such as hypermobility syndrome (HMS), and joint hypermobility syndrome (JHS) is a heritable connective tissue disorder [3] that affects joints and ligaments.
Joint hypermobility is often correlated with hypermobile Ehlers–Danlos syndrome (hEDS, known also by EDS type III or Ehlers–Danlos syndrome hypermobility type (EDS-HT)). Ehlers–Danlos syndrome is a genetic disorder caused by mutations or hereditary genes, but the genetic defect that produced hEDS is largely unknown.
Joint hypermobility is present, but generally confined to the small joints (fingers, toes). Other common features include club foot , tendon and/or muscle rupture, acrogeria (premature aging of the skin of the hands and feet), early-onset varicose veins , pneumothorax (collapse of a lung), the recession of the gums, and a decreased amount of ...
This creates normal joint stability. If muscular control does not compensate for ligamentous laxity, joint instability may result. The trait is almost certainly hereditary , and is usually something the affected person would just be aware of, rather than a serious medical condition.
Genetic conditions, such as hypermobility syndrome and Ehlers-Danlos syndrome put individuals at increased risk for dislocations. [13] Hypermobility syndrome is an inherited disorder that affects the ligaments around joints. [14] The loosened or stretched ligaments in the joint provide less stability and allow for the joint to dislocate more ...
Loeys–Dietz syndrome - autosomal dominant condition linked to a wide range of systemic manifestations, such as skeletal, cutaneous, vascular, and craniofacial abnormalities. [17] Hypermobility spectrum disorder - a variety of connective tissue diseases that are marked by ongoing pain and joint hypermobility. [18]
3. Sleep Deprivation. There is a link between sleep loss and weight gain. Research shows that people who routinely don’t get enough sleep tend to eat higher-calorie and higher-fat diets.. Not ...
This condition is considered to be rare, with about 1 in 100,000 births being affected by the congenital form of genu recurvatum, [3] although it's a common feature in some disorders, such as in joint hypermobility, which affects 1 in 30 people. [4]