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1 d connective tissue abnormalities, including joint hypermobility.
2 rs that have the orthopedic manifestation of joint hypermobility.
3 ene may account for some subgroups of benign joint hypermobility.
4 n syndrome, are characterized by generalized joint hypermobility.
5 abnormalities, gait/balance disturbance, and joint hypermobility.
6 e is a well-established relationship between joint hypermobility and anxiety in humans, that has not
7 s suggest a positive association between hip joint hypermobility and emotional arousal in domestic do
8 ) is characterized by an association between joint hypermobility and musculoskeletal pains, the latte
9 ncluding osteopenia, blue sclera, soft skin, joint hypermobility and neuromuscular junction dysfuncti
10 liosis, chest wall deformity, dural ectasia, joint hypermobility, and acetabular protrusion.
11 hat include feeding difficulties in infancy, joint hypermobility, and characteristic facial features
12 dontitis leading to premature loss of teeth, joint hypermobility, and mild skin findings.
13               A self-report questionnaire on joint hypermobility as well as data on age, height, weig
14 s provide hope that more common varieties of joint hypermobility can be understood and that effective
15 ctive tissue/myopathy overlap disorders with joint hypermobility, contractures, mild skeletal dysplas
16  clinical symptoms including gastric reflux, joint hypermobility, dysautonomia, flushing and pruritus
17    A subset of OI patients also present with joint hypermobility; however, the role of tendon dysfunc
18 otypes including progressive kyphoscoliosis, joint hypermobility, hypotonia, hyperelastic skin, heari
19 c factors have a substantial contribution to joint hypermobility in the adult female population.
20 underlie classic Ehlers-Danlos syndrome, and joint hypermobility is an important clinical manifestati
21                                              Joint hypermobility is widely prevalent in all communiti
22 onnective tissue, manifesting as early-onset joint hypermobility, joint contractures, muscle weakness
23                                    Extensive joint hypermobility, lower serum cartilage oligomeric ma
24                   Many conditions that cause joint hypermobility resolve with nonoperative management
25 permobility Ehlers-Danlos syndrome involving joint hypermobility, skin hyperelasticity, pain and gast
26 connective tissue disorders characterized by joint hypermobility, skin hyperelasticity, perivascular
27 vely inherited form of EDS (characterized by joint hypermobility, skin hyperextensibility, and cardia
28 ctive tissue, with common features including joint hypermobility, soft and hyperextensible skin, abno
29                                              Joint hypermobility syndrome (JHS) is characterized by a
30                                       Benign joint hypermobility syndrome, for example, shares simila
31 tional families, one of which diagnosed with joint hypermobility syndrome/Ehlers-Danlos syndrome hype
32 f speech, language, and behavior; hypotonia; joint hypermobility; visual system defects; and other co
33 and body mass index-adjusted heritability of joint hypermobility was estimated to be 70% (95% confide
34                                Whereas large-joint hypermobility was more common, lens dislocation an
35        Significantly greater concordance for joint hypermobility was observed in the MZ twins when co