Literature DB >> 17152113

Joint hypermobility.

Howard A Bird1.   

Abstract

Patients with joint hypermobility, perhaps the mildest of the various inherited abnormalities of connective tissue, may present to a rheumatologist or general practitioner although a large proportion are recognized by health professionals, particularly physiotherapists. Hypermobility may be generalized or extreme at a small number of joints. Sometimes it is associated with involvement of other organs because of abnormal inherited collagen structure elsewhere. A small proportion of patients will have one of the more serious conditions such as Ehlers-Danlos syndrome, Marfan's syndrome or osteogenesis imperfecta. Management is multidisciplinary requiring a team including physicians, physiotherapists, occupational therapists and podiatrists, among others. Patients often wait a long time before receiving their definitive diagnosis and are sometimes dismissed as malingerers. Patients often have a lot of queries about their condition unrelated to their joints. Among these are whether there will be problems in pregnancy, whether the condition will be passed on to their children, whether symptoms arising from organs other than the joints are related and whether they might have been incorrectly accused of battering their children.

Entities:  

Mesh:

Year:  2007        PMID: 17152113     DOI: 10.1002/msc.91

Source DB:  PubMed          Journal:  Musculoskeletal Care        ISSN: 1478-2189


  11 in total

1.  Association of hypermobility and ingrown nails.

Authors:  Fatma Gulru Erdogan; Abdurrahman Tufan; Munevver Guven; Berna Goker; Aysel Gurler
Journal:  Clin Rheumatol       Date:  2012-06-02       Impact factor: 2.980

2.  Is joint hypermobility important in prepubertal children?

Authors:  Pelin Yazgan; Iclal Geyikli; Dost Zeyrek; Lutfu Baktiroglu; Mehmet Ali Kurcer
Journal:  Rheumatol Int       Date:  2008-01-18       Impact factor: 2.631

3.  Prevalence, injury rate and, symptom frequency in generalized joint laxity and joint hypermobility syndrome in a "healthy" college population.

Authors:  Leslie N Russek; Deanna M Errico
Journal:  Clin Rheumatol       Date:  2015-05-01       Impact factor: 2.980

4.  Pain intensity and quality of life perception in children with hypermobility syndrome.

Authors:  Francis Fatoye; Shea Palmer; Fiona Macmillan; Philip Rowe; Marietta van der Linden
Journal:  Rheumatol Int       Date:  2011-01-26       Impact factor: 2.631

5.  The thumb carpometacarpal joint: anatomy, hormones, and biomechanics.

Authors:  Amy L Ladd; Arnold-Peter C Weiss; Joseph J Crisco; Elisabet Hagert; Jennifer Moriatis Wolf; Steven Z Glickel; Jeffrey Yao
Journal:  Instr Course Lect       Date:  2013

6.  Serum prolidase activity in benign joint hypermobility syndrome.

Authors:  Serda Em; Demet Ucar; Pelin Oktayoglu; Mehtap Bozkurt; Mehmet Caglayan; Ismail Yıldız; Osman Evliyaoglu; Kemal Nas
Journal:  BMC Musculoskelet Disord       Date:  2014-03-11       Impact factor: 2.362

7.  Adolescent obesity, joint pain, and hypermobility.

Authors:  Sharon Bout-Tabaku; Sarah B Klieger; Brian H Wrotniak; David D Sherry; Babette S Zemel; Nicolas Stettler
Journal:  Pediatr Rheumatol Online J       Date:  2014-03-29       Impact factor: 3.054

8.  Lumbar artificial disc replacement in Ehlers-Danlos syndrome: A case report and discussion of clinical management.

Authors:  Emily M Lindley; Brianna N Patti; Matthew Taylor; Evalina L Burger; Vikas V Patel
Journal:  Int J Spine Surg       Date:  2012-12-01

Review 9.  Managing the patient with osteogenesis imperfecta: a multidisciplinary approach.

Authors:  Caroline Marr; Alison Seasman; Nick Bishop
Journal:  J Multidiscip Healthc       Date:  2017-04-04

10.  Physical and mechanical therapies for lower limb symptoms in children with Hypermobility Spectrum Disorder and Hypermobile Ehlers-Danlos Syndrome: a systematic review.

Authors:  Benjamin Peterson; Andrea Coda; Verity Pacey; Fiona Hawke
Journal:  J Foot Ankle Res       Date:  2018-11-07       Impact factor: 2.303

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