Results 31 to 40 of about 1,081,004 (187)
Twin pregnancy with untyped Ehlers-Danlos syndrome requiring prompt genetic testing: A case report
Case Reports in Women's Health, 2022 Ehlers-Danlos syndrome is a rare genetic disorder that presents with a variety of pathologies depending on the disease type. Among them, vascular Ehlers-Danlos syndrome requires extremely careful management as there have been many reports of fatal ...
Shiori Ogawa +10 more
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Management of shoulder instability in hypermobility-type Ehlers-Danlos syndrome
JSES Reviews, Reports, and Techniques, 2021 Shoulder instability in hypermobile Ehlers-Danlos syndrome can result in lifelong pain and functional disability. Treatment in this population is complicated by the severe degree of instability as well as the underlying abnormalities of the joint ...
Samuel E. Broida, BS +3 more
doaj +1 more source
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
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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
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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
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.
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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
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
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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
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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
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