Titlebook: Hypermobility in Medical Practice; Neuseli Lamari,Peter Beighton Book 2023 The Editor(s) (if applicable) and The Author(s), under exclusiv

ACME

Contributors to the Understanding of the EDS and Hypermobility in Antiquity,ntributors to the understanding of Joint Hypermobility (JH). Notable individuals discussed in this chapter are Ehlers, Danlos and Parkes Weber. Current concepts are based upon early case reports concerning the Elhers-Danlos Syndrome in which an excessive range of joint movements is a major diagnosti

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Assessment of the Magnitude of Joint Hypermobility,ve been developed for the assessment of the extent and severity of Generalised Joint Hypermobility (GJH). The first method was proposed by Carter & Winkinson in 1964, who considered five articular movements. This was followed in 1970 by a method proposed by Beighton & Horan, using six articular move

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The Heterogeneity of Joint Hypermobility, common, while others are rare. In this chapter the various forms of Joint Hypermobility are outlined. In the last decade, growing attention has been given to joint hypermobility (JH) and related disorders. The new nosology for Ehlers-Danlos syndromes (EDS), which is the best known and probably the

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Mechanical Consequences of Joint Hypermobility,his chapter. Trunk instability occurs due to several factors, including muscle deficit with decreased strength, hypotrophy, muscle weakness, and fatigue. In addition to these influences, the weight of the trunk itself contributes to anterior tilt due to the lack of antigravitational musculature to k

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Ehlers-Danlos Syndromes,on criteria were established for hEDS in the absence of other collagen disorders. In this way, hypermobility spectrum disorders prioritise musculoskeletal manifestations in the presence of joint hypermobility. It is now evident that these are the same conditions which were established by Kirk, Ansel

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Joint Hypermobility Syndrome and Hypermobility Spectrum Disorders,rmobility spectrum disorders (HSDs) are a group of clinical conditions related to joint hypermobility (JH) that are descriptive and of diagnostic exclusion. They are used mainly as alternative labels for patients with symptomatic JH who do not meet the criteria of a variant of Ehlers-Danlos syndrome

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Joint Hypermobility in Newborns and Children,t is possible to identify early signs of JH in the form of habits and postures in the preclinical stages in affected newborns and children. However, the preclinical stages of JH in newborns are variable and may or may not emerge, depending on the conditions that characterize each phase. In other wor