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

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NATAL

Contributors to the Understanding of Hypermobility and Ehlers-Danlos Syndrome in the Modern Era,lity is presented in this chapter. The author, PB was acquainted with most of them and they were regarded as personal friends. Joint hypermobility or articular hyperlaxity is conventually defined by the Beighton score. This index is commonly used and perhaps the most reliable professional tool for e

neutrophils

braggadocio

The Heterogeneity of Joint Hypermobility,(hEDS). The concept of a spectrum of pathogenic manifestations related to JH was also concerning the categories of pleiotropic syndromes with JH. Thus, for several disorders in the hypermobility spectrum diagnostic labels were proposed for patients with symptomatic JH that do not correspond to any o

障礙

Biomechanical Aspects of Joint Hypermobility,e bundles of resistant fibers, which are fundamental in controlling movement by promoting stability to the joint. Stability of a ligament is obtained by the strength and elasticity of the collagen, which varies between individuals according to the inherited collagen structure. The human body adapts

使?jié)M足

locus-ceruleus

Ehlers-Danlos Syndromes,entifically validated in 1973 and is employed in both clinical practice and research. A numerical score derived from this method was developed during an epidemiological investigation in Africa. and remains among the current criteria for the diagnosis of EDS. Over time, clinicians and geneticists hav

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Joint Hypermobility in Different Periods of Life; An Overview,pment of the locomotor apparatus. The spinal column and limbs are mainly affected but abnormal facial features may occur, with consequent impairment of oral health. These factors can exert an influence on function and aesthetics throughout life. However, early recognition of JH is critical since it

Guileless

Joint Hypermobility in Newborns and Children,for secondary complications to develop and these can have implications for the patient and family throughout life. Physiotherapeutic care is important and should be initiated early to ensure a good aesthetic and functional prognosis. It is relevant that the recognition of JH in routine pediatric pra