Results 41 to 50 of about 19,422 (224)
Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome [PDF]
, 2015 Three international nosologies have been proposed for the diagnosis of Marfan syndrome (MFS): the Berlin nosology in 1988; the Ghent nosology in 1996 (Ghent-1); and the revised Ghent nosology in 2010 (Ghent-2).
Bannas, Peter +13 more
core +2 more sources
[Joint hypermobility syndrome].
Acta ortopedica mexicana, 2021 Joint hypermobility syndrome is an inherited disorder with autosomal dominant pattern; is characterized by joint hyperlaxity and musculoskeletal pains. Thermal hypermobility refers to the increase in active or passive movements of joints based on their normal ranges.
N, Carbonell-Bobadilla +5 more
openaire +2 more sources
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 +3 more
doaj +1 more source
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 +5 more
doaj +1 more source
Rehabilitation of shoulder impingement syndrome and rotator cuff injuries: an evidence-based review [PDF]
, 2010 Rehabilitation of the patient with glenohumeral impingement requires a complete understanding of the structures involved and the underlying mechanism creating the impingement response. A detailed clinical examination and comprehensive treatment programme
Cools, Ann, Ellenbecker, Todd S
core +1 more source
Defining Features of Gabriele‐de Vries Syndrome in Adults: A Case Report and Literature Review
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Gabriele‐de Vries syndrome (GADEVS) is a neurodevelopmental disorder caused by heterozygous pathogenic variants in the YY1 gene. Like most rare genetic syndromes, the adult manifestations of GADEVS remain poorly defined. Here, we describe the oldest patient reported to date with GADEVS—a 63‐year‐old woman with a c.1177_1179del YY1 variant ...
Ethan W. Hollingsworth, Changrui Xiao
wiley +1 more source
Venous insufficiency after prolonged standing: Is joint hypermobility an important risk factor?
Advanced 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
Validation of ankle strength measurements by means of a hand-held dynamometer in adult healthy subjects [PDF]
, 2017 Uniaxial Hand-Held Dynamometer (HHD) is a low-cost device widely adopted in clinical practice to measure muscle force. HHD measurements depend on operator’s ability and joint movements.
Ancillao, Andrea +2 more
core +2 more sources
Equine models in translational medicine: A comparative approach to human health
Animal Models and Experimental Medicine, EarlyView.This diagram summarizes and contrasts rodent and equine models, outlining their strengths, limitations, and applications. Horses offer naturally occurring diseases, genetic and physiological similarities to humans, and suitability for longitudinal and clinical‐scale studies.
Shayan Boozarjomehri Amnieh +1 more
wiley +1 more source
BMJ Open, 2022 Introduction Ehlers-Danlos syndromes (EDS)/generalised hypermobility spectrum disorders (G-HSD) affect the connective tissue of the body and present with a heterogeneous set of symptoms that pose a challenge for diagnosis.
Hance Clarke +4 more
doaj +1 more source