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The evidence-based rationale for physical therapy treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome.
Engelbert RH, Juul-Kristensen B, Pacey V, de Wandele I, Smeenk S, Woinarosky N, Sabo S, Scheper MC, Russek L, Simmonds JV. Engelbert RH, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):158-167. doi: 10.1002/ajmg.c.31545. Am J Med Genet C Semin Med Genet. 2017. PMID: 28306230 Free article.
New insights into the phenotype of Joint Hypermobility Syndrome (JHS) and Ehlers-Danlos Syndrome-hypermobile type (hEDS) have raised many issues in relation to classification, diagnosis, assessment, and treatment. Within the multidisciplinary team, physical thera …
New insights into the phenotype of Joint Hypermobility Syndrome (JHS) and Ehlers-Danlos Syndrome-hypermobile type (hEDS) have …
Diagnosis and Management of Hypermobility Spectrum Disorders in Primary Care.
Atwell K, Michael W, Dubey J, James S, Martonffy A, Anderson S, Rudin N, Schrager S. Atwell K, et al. J Am Board Fam Med. 2021 Jul-Aug;34(4):838-848. doi: 10.3122/jabfm.2021.04.200374. J Am Board Fam Med. 2021. PMID: 34312277 Free article. Review.
Hypermobility spectrum disorders (HSDs) encompass an array of connective tissue disorders characterized by joint instability and chronic pain. ...This article describes the incidence and prevalence, pathophysiology, diagnosis, and management of HSDs, including clini …
Hypermobility spectrum disorders (HSDs) encompass an array of connective tissue disorders characterized by joint instability a …
Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type compared to other heritable connective tissue disorders.
Colombi M, Dordoni C, Chiarelli N, Ritelli M. Colombi M, et al. Am J Med Genet C Semin Med Genet. 2015 Mar;169C(1):6-22. doi: 10.1002/ajmg.c.31429. Am J Med Genet C Semin Med Genet. 2015. PMID: 25821090 Review.
Joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type (JHS/EDS-HT) is an evolving and protean disorder mostly recognized by generalized joint hypermobility and without a defined molecular basis. ...
Joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type (JHS/EDS-HT) is an evolving and protean disorder …
Specifications and validation of the ACMG/AMP criteria for clinical interpretation of sequence variants in collagen genes associated with joint hypermobility.
Leone MP, Morlino S, Nardella G, Pracella R, Giachino D, Celli L, Baldo D, Turolla L, Piccione M, Salzano E, Busè M, Lastella P, Zollino M, Cantone R, Grosso E, Zonta A, Pasini B, Piscopo C, De Maggio I, Priolo M, Mammi C, Foiadelli T, Trabatti C, Savasta S, Iolascon A, Ferraris A, Lodato V, Di Giosaffatte N, Majore S, Selicorni A, Petracca A, Fusco C, Celli M, Guarnieri V, Micale L, Castori M. Leone MP, et al. Hum Genet. 2023 Jun;142(6):785-808. doi: 10.1007/s00439-023-02547-z. Epub 2023 Apr 20. Hum Genet. 2023. PMID: 37079061
A multidisciplinary team was set up for developing specifications of the ACMG/AMP criteria for COL1A1, COL1A2, COL2A1, COL3A1, COL5A1, COL5A2, COL11A1, COL11A2 and COL12A1, associated with various forms of HCTD featuring joint hypermobility, which is becoming one of …
A multidisciplinary team was set up for developing specifications of the ACMG/AMP criteria for COL1A1, COL1A2, COL2A1, COL3A1, COL5A1, COL5A …
Diagnosis and Treatment of Carpometacarpal Instability.
Warwick D, Fetouh S. Warwick D, et al. Hand Clin. 2022 May;38(2):261-268. doi: 10.1016/j.hcl.2021.11.005. Hand Clin. 2022. PMID: 35465943 Review.
Hypermobility of the first CMC joint may adversely affect hand function and may lead to osteoarthritis later in life. It presents more commonly in younger women with generalized joint hypermobility or postmenopausal women with early stages of arthritis …
Hypermobility of the first CMC joint may adversely affect hand function and may lead to osteoarthritis later in life. It prese …
The neuromuscular differential diagnosis of joint hypermobility.
Donkervoort S, Bonnemann CG, Loeys B, Jungbluth H, Voermans NC. Donkervoort S, et al. Am J Med Genet C Semin Med Genet. 2015 Mar;169C(1):23-42. doi: 10.1002/ajmg.c.31433. Am J Med Genet C Semin Med Genet. 2015. PMID: 25821091 Review.
Joint hypermobility is the defining feature of various inherited connective tissue disorders such as Marfan syndrome and various types of Ehlers-Danlos syndrome and these will generally be the first conditions to be considered by geneticists and pediatricians in the …
Joint hypermobility is the defining feature of various inherited connective tissue disorders such as Marfan syndrome and vario …
Editorial Commentary: Diagnosis and Treatment of Generalized Joint Hypermobility in Patients With Anterior Cruciate Ligament Injury.
Sundemo D, Senorski EH, Samuelsson K. Sundemo D, et al. Arthroscopy. 2021 Jul;37(7):2348-2350. doi: 10.1016/j.arthro.2021.03.052. Arthroscopy. 2021. PMID: 34226016
Generalized joint hypermobility (GJH), or laxity, is defined as hyperextensibility of the synovial joints. Hypermobility is caused by alterations in the connective tissues, in turn caused by various factors including impaired function of collagen proteins. .. …
Generalized joint hypermobility (GJH), or laxity, is defined as hyperextensibility of the synovial joints. Hypermobility …
Joint hypermobility as a distinctive feature in the differential diagnosis of myopathies.
Voermans NC, Bonnemann CG, Hamel BC, Jungbluth H, van Engelen BG. Voermans NC, et al. J Neurol. 2009 Jan;256(1):13-27. doi: 10.1007/s00415-009-0105-1. Epub 2009 Feb 9. J Neurol. 2009. PMID: 19221853 Review.
We therefore present an overview of myopathies associated with joint hypermobility: Ullrich congenital muscular dystrophy, Bethlem myopathy, congenital muscular dystrophy with joint hyperlaxity, multi-minicore disease, central core disease, and limb girdle mu …
We therefore present an overview of myopathies associated with joint hypermobility: Ullrich congenital muscular dystrophy, Bet …
Efficacy of prolotherapy and arthrocentesis in management of temporomandibular joint hypermobility.
Taşkesen F, Cezairli B. Taşkesen F, et al. Cranio. 2023 Sep;41(5):423-431. doi: 10.1080/08869634.2020.1861887. Epub 2020 Dec 16. Cranio. 2023. PMID: 33326351
OBJECTIVE: The aim of this study was to compare the efficacy of dextrose prolotherapy in conjunction with arthrocentesis and dextrose prolotherapy alone in the management of symptomatic TMJ hypermobility. METHODS: Twenty-four patients suffering from TMJ symptomatic hype …
OBJECTIVE: The aim of this study was to compare the efficacy of dextrose prolotherapy in conjunction with arthrocentesis and dextrose prolot …
Diagnostic outcomes for molecular genetic testing in children with suspected Ehlers-Danlos syndrome.
Damseh N, Dupuis L, O'Connor C, Oh RY, Wang YW, Stavropoulos DJ, Schwartz SB, Mendoza-Londono R. Damseh N, et al. Am J Med Genet A. 2022 May;188(5):1376-1383. doi: 10.1002/ajmg.a.62672. Epub 2022 Feb 6. Am J Med Genet A. 2022. PMID: 35128800
In this retrospective study, we reviewed 72 patients referred to a tertiary care center for evaluation of EDS who underwent one or more forms of genetic testing. ...Fifty-four patients (54/72, 75%) had features that overlapped EDS and other syndromes associated with joi …
In this retrospective study, we reviewed 72 patients referred to a tertiary care center for evaluation of EDS who underwent one or mo …
66 results