Results 71 to 80 of about 1,476,694 (213)

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

Combinations to define generalized joint hypermobility.

Combinations to define generalized joint hypermobility.
Christina B. Olsson (17140285), Lena Nilsson-Wikmar (5863346), Per Kristiansson (707526), Angela Schlager (5863340), Kerstin Ahlqvist (5863343)   +4 more
core   +1 more source

Physical therapy of children with particular systemic lesion based on the undifferentiated connective tissue dysplasia

Слобожанський науково-спортивний вісник, 2019
Purpose: to develop and prove the effectiveness of a comprehensive physical therapy program for children with systemic visual and musculoskeletal lesions based on the undifferentiated connective tissue dysplasia.
Yuliia Rudenko, Oleksandr Zviriaka, Yuliia Arieshyna   +2 more
doaj   +1 more source

Inducible Laryngeal Obstruction in Hypermobile Patients

The Laryngoscope, EarlyView.
Patients with hypermobile Ehlers‐Danlos syndrome (hEDS) or hypermobility spectrum disorders (HSD) who screened positive for inducible laryngeal obstruction (ILO) reported significantly greater voice, cough, swallowing, gastrointestinal, and mast cell‐related symptoms than those without ILO. Chronic cough, dysphagia, and elevated mast cell symptom score
Stacey M. Menton, DeLisa Fairweather, Frances C. Wilson, Derek J. Zangerle, Emma F. Murphy, Ashley A. Darakjian, Chandler C. Thompson, Shilpa N. Gajarawala, Dacre R. T. Knight, Katelyn A. Bruno, Amy L. Rutt   +10 more
wiley   +1 more source

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

Movement 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, Brian Steele, Megan Howlett, Kate Kain, Davide Martino, Kimberly G. Williams, Gabriela S. Gilmour   +6 more
wiley   +1 more source

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

, 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

The mitral valve prolapse frequency in healthy females with generalized joint hypermobility: A case-control study

The Turkish Journal of Gastroenterology, 2021
Objectives: The aim of this study was to investigate the frequency of mitral valve prolapse between healthy females with generalized joint hypermobility and healthy controls. Patients and methods: This observational, cross-sectional, controlled study
Hande Özdemir, Filiz Tuna, Meryem Aktoz, Nurettin Taştekin, Derya Demirbağ Kabayel   +4 more
doaj  

DIFFERENTIATED INFRASTRUCTURAL CITIZENSHIP: Claims‐Making and the Limits to Transformative Urbanization in a Fast‐Growing Small City

International Journal of Urban and Regional Research, EarlyView.
Abstract This article develops the concept of differentiated infrastructural citizenship (DIC) to explain how infrastructural citizenship is materially mediated, socially differentiated, and unevenly exercised in a rapidly urbanizing small city. It advances scholarship on infrastructural citizenship and everyday claims‐making as political participation
Nidhi Subramanyam
wiley   +1 more source

Comparative diagnostic challenges in two horses with skin fragility disorders

Equine 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, F. A. Saiki, T. G. Cristo, M. C. Silva, R. J. Souza, A. F. Souza, R. A. Casagrande, J. H. Fonteque, C. I. G. Vogel   +8 more
wiley   +1 more source

Risk Factors and Clinical Severity in Chronic Venous Disease: A New Look

International Journal of Dermatology, EarlyView.
Genetic factors, such as gender and positive family history, were associated with the occurrence of mild‐stage disease (CEAP C1–3). Obesity, lack of exercise, and working more than 8 h in a sitting or standing position are strongly associated with severe venous disease (CEAP C4–6).
Éva Badak, Eszter A. Janka, Patrícia Ari, Edina Bodnár, Krisztina Varga, László Virág, Éva Szabó   +6 more
wiley   +1 more source