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Knowledge, assessment, and management of adults with joint hypermobility syndrome/Ehlers–Danlos syndrome hypermobility type among flemish physiotherapists

open access: yesAmerican Journal of Medical Genetics, Part C: Seminars in Medical Genetics, 2015
Physiotherapy plays a fundamental role in managing adults with the joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type (JHS/EDS-HT).
Jane Simmonds   +2 more
exaly   +2 more sources
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Gastrointestinal and nutritional issues in joint hypermobility syndrome/ehlers–danlos syndrome, hypermobility type

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2015
Gastrointestinal involvement is a well known complication of Ehlers–Danlos syndromes (EDSs), mainly in form of abdominal emergencies due to intestinal/abdominal vessels rupture in vascular EDS. In the last decade, a growing number of works investigated the relationship between a wide spectrum of chronic gastrointestinal complaints and various EDS forms,
Castori M   +4 more
openaire   +2 more sources

THE EFFECT OF THE HYPERMOBILITY SYNDROME ON KNEE JOINT PROPRIOCEPTION

Rheumatology, 1995
Proprioceptive sensory feedback is utilized by the central nervous system for conscious appreciation of the position and movement of the body and limbs. In patients with the hypermobility syndrome (HMS), it has been suggested that there is alteration of proprioceptive acuity.
M G, Hall   +4 more
openaire   +2 more sources

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
openaire   +1 more source

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
openaire   +2 more sources

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
openaire   +2 more sources

Spectrum of Gastrointestinal Manifestations in Joint Hypermobility Syndromes

The American Journal of the Medical Sciences, 2018
Joint hypermobility is a common, primarily benign finding in the general population. However, in a subset of individuals joint hypermobility causes a range of clinical problems mainly affecting the musculoskeletal system and, to a lesser extent, extra-articular disorders.
Gehan, Botrus   +8 more
openaire   +2 more sources

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
openaire   +2 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
openaire   +2 more sources

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