Results 31 to 40 of about 1,247,077 (145)
Fascial thickness and stiffness in hypermobile
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2021 AbstractThere is a high prevalence of myofascial pain in people with hypermobile Ehlers‐Danlos Syndrome (hEDS). The fascial origin of pain may correspond to changes in the extracellular matrix. The objective of this study was to investigate structural changes in fascia in hEDS.
Tina J. Wang, Antonio Stecco
openaire +2 more sources
Rupture of abdominal aortic aneurysm after spine surgery in the patient with Ehlers-Danlos syndrome -A case report- [PDF]
Korean Journal of Anesthesiology, 2010 Ehlers-Danlos syndrome (EDS) is a rare inherited disorder of the connective tissue that is characterized by hyperextensible skin, hypermobile joints and abnormalities of the cardiovascular system.
Jung Sik Im +4 more
doaj +1 more source
Chronic fatigue in Ehlers–Danlos syndrome—Hypermobile type [PDF]
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2017 Chronic fatigue is an important contributor to impaired health‐related quality of life in Ehlers–Danlos syndrome. There is overlap in the symptoms and findings of EDS and chronic fatigue syndrome. A proportion of those with CFS likely have EDS that has not been identified.
Alan, Hakim +4 more
openaire +2 more sources
Comorbidity between Autism Spectrum Disorders and hypermobile Ehlers-Danlos syndrome
, 2021 The main goal of this study is to assess the comorbidity between hypermobile Ehlers-Danlos Syndrome (hEDS) symptoms and Autism Spectrum disorders (ASD ...
Morgane Burnel
core +1 more source
An acquired or heritable connective tissue disorder? a review of hypermobile Ehlers Danlos Syndrome [PDF]
, 2019 Hypermobile Ehlers Danlos Syndrome (hEDS) is a multifaceted disorder that is difficult to diagnose and manage primarily due to the unknown causes. Research on hEDS continues to evolve but tangible progress will be realized when the growing body of ...
Martin, A.
core +1 more source
THE DIFFERENTIAL DIAGNOSIS OF CHILDREN WITH JOINT HYPERMOBILITY: A REVIEW OF THE LITERATURE [PDF]
Romanian Journal of Pediatrics, 2009 Background. In this study we aimed to identify and review publications relating to the diagnosis of joint hypermobility and instability and develop an evidence based approach to the diagnosis of children presenting with joint hypermobility and related ...
Louise J. Tofts +4 more
doaj +3 more sources
Clinical Case Reports, 2022 A young male patient presents with widespread pain and varying chronic inflammatory symptoms for three years and idiopathic low bone density for more than ten years.
Cameron Rattray
doaj +1 more source
Annals of Internal Medicine: Clinical Cases, 2023 Loeys–Dietz syndrome (LDS) 5 is characterized by aortic aneurysms, hypertelorism, and cleft palate/bifid uvula. We describe a woman with a transforming growth factor beta3 (TGFβ3) mutation who displays a forme fruste phenotype of LDS5.
Tarika D. Patel +2 more
doaj +1 more source
Frontiers in Medicine, 2023 Patients with hypermobile Ehlers-Danlos syndrome (hEDS) frequently suffer from poor balance and proprioception and are at an increased risk for falls.
Miguel Whitmore +8 more
doaj +1 more source
, 2022 This project will involve surveying adults from the United States who are diagnosed with hypermobile Ehlers-Danlos Syndrome (hEDS) or hypermobility spectrum disorder (HSD) or individuals who suspect they have one of these conditions. Participants will be
Pat Frazier +3 more
core +1 more source