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Benign Joint Hypermobility Syndrome

2021
Benign joint hypermobility syndrome (BJHS) is frequently encountered in the community. Joint hypermobility by itself is not enough to diagnose BJHS. Not all patients with joint hypermobility go on to develop joint hypermobility syndrome. The diagnosis of BJHS requires the presence of musculoskeletal pain in addition to joint hypermobility. The Beighton
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Symptom and joint mobility progression in the joint hypermobility syndrome (Ehlers-Danlos syndrome, hypermobility type).

Clinical and experimental rheumatology, 2011
To evaluate progression of symptoms and joint mobility in the joint hypermobility syndrome (JHS) in order to identify specific disease pictures by age at presentation.Fifty JHS patients (44 females, 6 males) were evaluated by Beighton score (BS) calculation, and presence/absence and age at onset of 20 key symptoms. Incidence and prevalence rates by age
CASTORI, MARCO   +4 more
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The joint hypermobility syndrome in a Cuban juvenile population

Reumatología Clínica (English Edition), 2009
In order to review the rise in joint hypermobility syndrome, identify the patterns associated with this diagnosis and correlate its most relevant symptoms, we did a descriptive transversal analytic study in a group of 280 young people of both genders between 15 and 17 years of age.
Francisco M, Menéndez Alejo   +3 more
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Hypermobility and joint hypermobility syndrome in Brazilian students and teachers of ballet dance

Rheumatology International, 2014
The current literature has been discussing the risks and benefits of joint hypermobility (JHM) for careers in ballet This study aimed to evaluate the prevalence of JHM and joint hypermobility syndrome (JHS) in a group of ballet teachers and students, looking both at aspects related to the flexibility required to dance, as at the risk of injuries when ...
S B, Sanches   +4 more
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The lack of clinical distinction between the hypermobility type of Ehlers–Danlos syndrome and the joint hypermobility syndrome (a.k.a. hypermobility syndrome)

American Journal of Medical Genetics Part A, 2009
The Lack of Clinical Distinction Between the Hypermobility Type of Ehlers–Danlos Syndrome and the Joint Hypermobility Syndrome (a.k.a. Hypermobility Syndrome) Brad T. Tinkle,* Howard A. Bird, Rodney Grahame, Mark Lavallee, Howard P. Levy, and David Sillence Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio University of Leeds, West ...
Brad T, Tinkle   +5 more
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Joint hypermobility syndrome for the urogynaecologist – A narrative review

European Journal of Obstetrics & Gynecology and Reproductive Biology
Joint Hypermobility Syndrome (JHS), also referred to as hypermobile Ehlers-Danlos Syndrome (hEDS), is increasingly recognised as a significant contributor to gynaecological, pelvic floor and lower urinary tract symptoms. This review aims to highlight the current evidence on the relationship between JHS and key urogynaecological conditions, with ...
Islam, Abaza   +5 more
openaire   +2 more sources

Joint Hypermobility Syndromes and the Spine

Contemporary Neurosurgery, 2011
Charles J. Wrobel, Eric M. Thompson
  +4 more sources

Joint hypermobility as a manifestation of neonatal Sotos syndrome

BMJ Case Reports
Summary Sotos syndrome is associated with hypergrowth, macrocephaly, intellectual disability and characteristic facial features, the diagnosis of which becomes more evident during childhood. We present the case of a full-term newborn, who was admitted to the Neonatology Unit with early hypoglycaemia, hypotonia, a peculiar phenotype ...
Vanesa Botella López   +3 more
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JOINT HYPERMOBILITY SYNDROME AND ANXIETY DISORDERS

The Lancet, 1988
A, Bulbena   +4 more
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