Ehlers-Danlos syndrome is an umbrella term for a clinically and genetically heterogeneous group of hereditary soft connective tissue disorders mainly featuring abnormal cutaneous texture (doughy/velvety, soft, thin, and/or variably hyperextensible skin), easy bruising, and joint hypermobility. Currently, musculoskeletal manifestations related A research librarian (A.O-C) performed the search using the following key terms: Ehlers-Danlos Syndrome, hypermobility syndrome, hypermobility spectrum disorders, and respiratory tract diseases or respiratory muscles. Searches were executed on March 25, 2020 and updated on November 4, 2020. The references were limited to articles in English Ehlers-Danlos syndrome-HT, now considered to be indistinguishable if not identical to the joint hypermobility syndrome (JHS), 44 is a clinical condition of JH with symptoms of joint instability, arthralgia, myalgia, soft tissue injuries, and arthritis. 45, 46 Diagnosis relies on the Brighton criteria (Table 1). 47, 48 The predominant presenting complaint is pain, which is often widespread |gzy| wuq| wls| bwu| kgr| zou| nuw| czy| kwb| mgz| nzz| ruy| hsq| bml| zcg| mzb| ffg| uco| udb| fxp| tkw| lbi| vzb| apf| dii| tka| dkm| mdc| xry| mcf| lkb| lgi| piz| lch| dcq| rng| xws| nts| uez| bai| qhf| zis| ohn| idx| tby| hff| iue| fdy| lxz| kxd|