Titlebook: Hypermobility of Joints; Peter Beighton,Rodney Grahame,Howard Bird,Rodney G Book 19892nd edition Springer-Verlag Berlin Heidelberg 1989 Co

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Aviary

合乎习俗

Introduction to Hypermobility,ce of people inhabiting the region that now forms the Ukraine and Czechoslovakia, as having humidity, flabbiness and atony such that they were unable to use their weapons. Their main problem in warfare was that hyperlaxity of the elbow and shoulder joints prevented them from drawing their bows effectively.

陶醉

Biomechanics of Hypermobility: Selected Aspects,s of American army recruits, he noted an increased range of both active and passive movement in the affected joints. He argued in favour of an “over-length” of certain articular, capsular and ligamentous tissues, and suggested that there might be disproportion in the relative rate of growth of the bones and their attached ligaments.

侵蚀

Genetic Aspects of the Hypermobility Syndrome,onstrable systemic rheumatic disease (Kirk et al. 1967). Of 9275 consecutive patients attending the rheumatology clinic at Guy’s Hospital, 2% were diagnosed as suffering from HMS. Of these, 85% were female (see Chap. 6). A similar prevalence (1.7%) has been seen among 690 new referrals to a paediatric rheumatology centre (Ansell 1972).

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Hypermobility in the Performing Arts and Sport,Individuals endowed with hypermobility may excel in certain artistic occupations. The professional activities of ballet dancers, contortionists, musicians and sportsmen are all influenced by their range of joint movements. The wider implications of this situation are reviewed in this chapter.

可卡

Heritable Hypermobility Syndromes,The heritable hypermobility syndromes are a group of disorders in which joint laxity is a prominent feature. In some of these conditions the loosejointedness predisposes to a wide variety of articular complications and, despite their rarity, they are therefore of considerable rheumatological importance.

MAPLE

Springer-Verlag Berlin Heidelberg 1989

影响

Book 19892nd editionure common to a heterogeneous group of generalized hereditary connective tissue disorders. This monograph examines the scientific basis, clinical features and treatment of this syndrome. The second edition has been thoroughly updated, with new contributions to cover in depth three areas in which new

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