Joint hypermobility and genetic collagen disorders: are they related?

被引:199
作者
Grahame, R [1 ]
机构
[1] UCL Hosp, Hypermobil Clin, London W1P 9PG, England
关键词
D O I
10.1136/adc.80.2.188
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The HDCTs constitute a heterogeneous group of rare genetically determined diseases, the best known of which are Elders-Danlos and Marfan syndromes and osteogenesis imperfecta. Hypermobility is a feature common to them all, but it is also a feature that is highly prevalent in the population at large. Symptomatic hypermobile subjects (whose symptoms are attributable to their hypermobility) are said to be suffering from the benign joint hypermobility syndrome, which has many features that overlap with the HDCTs. It is not yet known whether there is a variety of hypermobility (symptomatic or otherwise) that is not part of a connective tissue disorder.
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页码:188 / 191
页数:4
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