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1 ctors (such as muscle weakness, obesity, and joint laxity).
2 ly used to establish a clinical diagnosis of joint laxity.
3 ctors, such as muscle weakness, obesity, and joint laxity.
4 ity type of EDS, a condition marked by gross joint laxity and chronic musculoskeletal pain.
5 etaphyseal dysplasia, short-limbed dwarfism, joint laxity and early onset osteoarthritis.
6 es III or IV OI, plus severe large and small joint laxity and early progressive scoliosis.
7 ias characterized by variable short stature, joint laxity and early-onset degenerative joint disease.
8                                              Joint laxity and low muscle tone contributed to musculos
9 e issues, mechanical characteristics such as joint laxity and malalignment, and radiographic severity
10 re condition characterized by short stature, joint laxity, and advanced carpal ossification.
11 pe littermates and display gait abnormality, joint laxity, and age-dependent osteoarthritis.
12 sed body size, grip weakness, abnormal gait, joint laxity, and early-onset osteoarthritis.
13 mphysema, inguinal and diaphragmatic hernia, joint laxity, and pectus excavatum by age 2 years.
14 e disorders characterized by skin fragility, joint laxity, and skeletal deformities.
15 fness compared with controls consistent with joint laxity in EDS patients.
16 me tendon weakness are the likely causes for joint laxity in the double-nulls.
17        Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type (lepto-SEMDJL, aka SEMD
18 eness of subtle hypermobility or symptomatic joint laxity on physical examination facilitates optimal
19 siblings with progressive neurodegeneration, joint laxity, skin hyperelasticity and bilateral subcaps

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