Results 31 to 40 of about 2,102,167 (192)

Gait biomechanics in joint hypermobility syndrome: A spatiotemporal, kinematic and kinetic analysis [PDF]

, 2020
IntroductionJoint hypermobility syndrome (JHS) symptoms of widespread joint hypermobility and pain, muscle weakness and reduced muscle‐tendon stiffness suggest that there may be an impact on gait parameters.
Palmer, Shea, Cramp, Mary, Najla Alsiri, Sue Barnett, Shea Palmer, Alsiri, Najla, Barnett, Sue, Mary Cramp   +7 more
core   +1 more source

Síndrome da hipermobilidade articular em jovem

Galicia Clínica, 2016
Joint hypermobility syndrome (JHS) is a hereditary connective tissue disorder characterized by symptomatic generalized joint hypermobility. Other features such as luxations and subluxations, periarticular lesions and cutaneous or other organ ...
Joana Neves, Inês Cunha, Renata Aguiar, Anabela Barcelos   +3 more
doaj   +1 more source

Prevalence of generalized joint hypermobility in children with anxiety disorders

BMC Musculoskeletal Disorders, 2020
Background Concerning the high prevalence of anxiety disorders and joint hypermobility in children and the lack of related studies in this age group, we aimed to assess the association of hypermobility with anxiety disorders in children.
Vadood Javadi Parvaneh, Shadialsadat Modaress, Ghazal Zahed, Khosro Rahmani, Reza Shiari   +4 more
doaj   +1 more source

Relations between the occurrence of hypermobility and gender in the group of children aged 6 - 10 years

Journal of Education, Health and Sport, 2018
Introduction:Hypermobility of joints in healthy people may be either acquired or congenital be a symptom of a connective tissue disorder such as Marfan syndrome, osteogenesis imperfecta, or Ehler-Danlos syndrome.
Joanna Maryczkanicz, Katarzyna Weber-Nowakowska   +1 more
doaj   +3 more sources

The Prevalence of Undifferentiated Connective Tissue Dysplasia in Senior Students

Reabilitacijos Mokslai: Slauga, Kineziterapija, Ergoterapija, 2023
Background. Connective tissue dysplasia is an important medical condition requiring attention and research. The aim. To analyse the prevalence of the clinical signs of undifferentiated connective tissue dysplasia among senior students of educational ...
Mykhailo Protsailo , Volodymyr Dzhyvak , Ihor Krycky, Pavlo Hoshchynskyi, Ihor Horishnyi , Iryna Chornomydz   +5 more
doaj   +1 more source

Physical and mechanical therapies for lower limb symptoms in children with Hypermobility Spectrum Disorder and Hypermobile Ehlers-Danlos Syndrome: a systematic review

Journal of Foot and Ankle Research, 2018
Background Hypermobility Spectrum Disorder and Hypermobile Ehlers Danlos Syndrome are two common heritable genetic disorders of connective tissue. Both conditions are characterised by excessive joint range of motion and the presence of musculoskeletal ...
Benjamin Peterson, Andrea Coda, Verity Pacey, Fiona Hawke   +3 more
doaj   +1 more source

Ocular and Systemic Findings in COL2A1 and COL11A1 Stickler Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Stickler syndrome is most commonly caused by variants in COL2A1 and COL11A1 genes. The purpose of this study was to describe genetic variants and phenotypes in COL2A1 and COL11A1 Stickler syndrome. We performed a retrospective genotype–phenotype evaluation of COL2A1 and COL11A1 Stickler syndrome subjects. Thirty‐two subjects with COL2A1 and 13
Aileen G. MacLachlan, Jessica A. Kraker, Denise J. Morgan, Lisa A. Schimmenti, M. Elizabeth Hartnett, Eileen S. Hwang   +5 more
wiley   +1 more source

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

, 2010
Evidence suggests that developmental coordination disorder (DCD) co-occurs with attention deficit hyperactivity disorder (ADHD) and joint hypermobility syndrome (JHS).
Sparks, J., Amanda Kirby, Karina Baudinette, Baudinette, K., Kirby, A., Jennie Sparks   +5 more
core   +1 more source

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway — A Description of Demographic, Medical, and Neurological Findings

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen, Kristin Ørstavik, Unni Steen, Mathias Toft, Cathrine Brunborg, Lena Lande Wekre   +5 more
wiley   +1 more source

The effects of joint hypermobility syndrome on the kinematics and kinetics of the vertical jump test [PDF]

, 2020
Purpose: Biomechanical impairments are not apparent during walking in people with Joint Hypermobility Syndrome (JHS). This research explored biomechanical alterations during a higher intensity task, vertical jumping.
Palmer, Shea, Cramp, Mary, Alsiri, Najla, Barnett, Sue   +3 more
core   +1 more source