Literature DB >> 18221908

Hypermobility and the hypermobility syndrome, part 2: assessment and management of hypermobility syndrome: illustrated via case studies.

Jane V Simmonds1, Rosemary J Keer.   

Abstract

Joint hypermobility syndrome (JHS) is a largely under-recognised and poorly understood multi-systemic hereditary connective tissue disorder which manifests in a variety of different clinical presentations. The assessment and management of patients with the syndrome is often complicated, requiring a comprehensive patient-centred approach and co-ordinated input from a range of medical, health and fitness professionals. The functional rehabilitation process is frequently lengthy, with education of the patient and family, sensitively prescribed and monitored physical therapy interventions and facilitation of lifestyle and behaviour modifications being the mainstay of the plan. Two typical but very different case studies are presented, each illustrating key aspects of the assessment and highlighting the variety of management strategies and techniques required by therapists to facilitate successful outcomes.

Entities:  

Mesh:

Year:  2008        PMID: 18221908     DOI: 10.1016/j.math.2007.11.001

Source DB:  PubMed          Journal:  Man Ther        ISSN: 1356-689X


  14 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.  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

3.  Multimodal chiropractic care of pain and disability for a patient diagnosed with benign joint hypermobility syndrome: a case report.

Authors:  Richard G Strunk; Mark T Pfefer; Derrick Dube
Journal:  J Chiropr Med       Date:  2014-03

4.  An investigation of the control of quadriceps in people who are hypermobile; a case control design. Do the results impact our choice of exercise for people with symptomatic hypermobility?

Authors:  Michael Long; Louise Kiru; Jamila Kassam; Paul H Strutton; Caroline M Alexander
Journal:  BMC Musculoskelet Disord       Date:  2022-06-23       Impact factor: 2.562

Review 5.  Joint hypermobility syndrome pain.

Authors:  Rodney Grahame
Journal:  Curr Pain Headache Rep       Date:  2009-12

6.  Generalized Joint Laxity is Associated with Primary Occurrence and Treatment Outcome of Lumbar Disc Herniation.

Authors:  Woo Jin Han; Hong-Bae Kim; Gun Woo Lee; Jung Heum Choi; Won Jin Jo; Sun-Mi Lee
Journal:  Korean J Fam Med       Date:  2015-05-22

Review 7.  Hypermobile Ehlers-Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes.

Authors:  Cortney Gensemer; Randall Burks; Steven Kautz; Daniel P Judge; Mark Lavallee; Russell A Norris
Journal:  Dev Dyn       Date:  2020-08-17       Impact factor: 3.780

8.  Ehlers-danlos syndrome, hypermobility type: an underdiagnosed hereditary connective tissue disorder with mucocutaneous, articular, and systemic manifestations.

Authors:  Marco Castori
Journal:  ISRN Dermatol       Date:  2012-11-22

9.  Exercise in children with joint hypermobility syndrome and knee pain: a randomised controlled trial comparing exercise into hypermobile versus neutral knee extension.

Authors:  Verity Pacey; Louise Tofts; Roger D Adams; Craig F Munns; Leslie L Nicholson
Journal:  Pediatr Rheumatol Online J       Date:  2013-08-14       Impact factor: 3.054

10.  Children with generalised joint hypermobility and musculoskeletal complaints: state of the art on diagnostics, clinical characteristics, and treatment.

Authors:  M C Scheper; R H H Engelbert; E A A Rameckers; J Verbunt; L Remvig; B Juul-Kristensen
Journal:  Biomed Res Int       Date:  2013-07-22       Impact factor: 3.411

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