Results 51 to 60 of about 2,646,959 (190)

Survey of Paediatric Occupational Therapists' Understanding of Developmental Coordination Disorder, Joint Hypermobility Syndrome and Attention Deficit Hyperactivity Disorder

open access: yes, 2010
Evidence suggests that developmental coordination disorder (DCD) co-occurs with attention deficit hyperactivity disorder (ADHD) and joint hypermobility syndrome (JHS).
Sparks, J.   +5 more
core   +1 more source

Deep stabilization muscles training in patients with polyarticular hypermobility

open access: yesJournal of Education, Health and Sport, 2017
Hypermobility syndrome is an inherited dysfunction in the structure of connective tissues. It is manifested by disturbances in the proportion of collagen.
Magdalena Gębska   +4 more
doaj   +3 more sources

From Disability to Diagnosis: Baseline Findings from the Calgary Functional Movement Disorder Registry

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background Functional movement disorder (FMD), a subtype of functional neurological disorder, is a complex neuropsychiatric syndrome characterized by inconsistent and incongruent motor symptoms. Despite its relatively high prevalence, FMD remains associated with delayed diagnosis, significant disability, and limited evidence to guide ...
Andrea Soumbasis   +6 more
wiley   +1 more source

Venous insufficiency after prolonged standing: Is joint hypermobility an important risk factor?

open access: yesAdvanced Biomedical Research, 2015
Background: Varicose veins are extremely common disease which is due to elevated superficial venous pressures. We aimed to know that if joint hypermobility causes the venous insufficiency following the prolonged standing.
Kamran Azma   +4 more
doaj   +1 more source

Comparative diagnostic challenges in two horses with skin fragility disorders

open access: yesEquine Veterinary Education, EarlyView.
Summary Hereditary equine regional dermal asthenia (HERDA) is an autosomal recessive connective tissue disorder of horses caused by a missense mutation (c.115G>A) in the peptidyl‐prolyl cis–trans isomerase B (PPIB) gene, resulting in defective collagen organisation.
M. Biolchi   +8 more
wiley   +1 more source

Expanding the Clinical Spectrum of DHX30‐Related Neurodevelopmental Disorder: A Case Report and a Scoping Review

open access: yesJournal of Intellectual Disability Research, EarlyView.
ABSTRACT Background Whole exome sequencing (WES) has improved diagnostic rates for neurodevelopmental disorders (NDDs) while introducing challenges in novel variant interpretation. DHX30‐related NDD (DHX30‐NDD) is a recently described condition with an evolving phenotypic spectrum.
Nattaporn Tassanakijpanich   +3 more
wiley   +1 more source

Prevalence of joint hypermobility, hypermobility spectrum disorder and hypermobile Ehlers-Danlos syndrome in a university population: an observational study

open access: yes, 2020
Objectives: To investigate the prevalence of joint hypermobility classes, hypermobility spectrum disorders,hypermobile Ehlers-Danlos syndrome and their relations with sex ina university population.
Filiz TUNA, Tuna, Filiz
core   +1 more source

Long COVID and hypermobility spectrum disorders have shared pathophysiology

open access: yesFrontiers in Neurology
Hypermobility spectrum disorders (HSD) and hypermobile Ehlers–Danlos syndrome (hEDS) are the most common joint hypermobility conditions encountered by physicians, with hypermobile and classical EDS accounting for >90% of all cases.
Ravindra Ganesh, Bala Munipalli
doaj   +1 more source

Quality of Online Information for Management of Leg Pain in Children and Adolescents With Hypermobility‐Associated Conditions

open access: yesJournal of Paediatrics and Child Health, EarlyView.
ABSTRACT Aim Online health information seeking continues to gain popularity. Quality assessment of online information is particularly important for patient populations with low satisfaction and disengagement from health professionals and services, such as hypermobility‐associated conditions.
R. Quinlan   +4 more
wiley   +1 more source

Genetic risk variants implicate impaired maintenance and repair of periodontal tissues as causal for periodontitis—A synthesis of recent findings

open access: yesPeriodontology 2000, EarlyView.
AbstractPeriodontitis is a complex inflammatory disease in which the host genome, in conjunction with extrinsic factors, determines susceptibility and progression. Genetic predisposition is the strongest risk factor in the first decades of life. As people age, chronic exposure to the periodontal microbiome puts a strain on the proper maintenance of ...
Arne S. Schaefer   +4 more
wiley   +1 more source

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