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Suicidal Behaviors in Women With the Hypermobile Ehlers–Danlos Syndrome

Archives of Suicide Research, 2021
Hypermobile Ehlers-Danlos syndrome (hEDS) is the most frequent heritable disorder of the connective tissue. This is characterized by a generalized fragility of tissues leading to chronic pain, disability and high levels of psychological distress. Suicidal behaviors in those affected are not uncommon but they have not been well studied.
Baeza-Velasco, Carolina   +3 more
openaire   +2 more sources

Prevalence of hypermobile Ehlers-Danlos syndrome in postural orthostatic tachycardia syndrome

open access: yesAutonomic Neuroscience: Basic and Clinical, 2020
Despite well-established clinical associations between Hypermobile Ehlers-Danlos syndrome (hEDS) and postural orthostatic tachycardia syndrome (POTS), the precise prevalence is unknown. We therefore evaluated for hEDS in 91 POTS participants using the 2017 hEDS diagnostic checklist, which has three major criteria: 1) generalized joint hypermobility ...
Amanda J Miller   +2 more
exaly   +4 more sources

Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history [PDF]

open access: yesAmerican Journal of Medical Genetics, Part C: Seminars in Medical Genetics, 2017
The hypermobile type of Ehlers–Danlos syndrome (hEDS) is likely the most common hereditary disorder of connective tissue. It has been described largely in those with musculoskeletal complaints including joint hypermobility, joint subluxations/dislocations, as well as skin and soft tissue manifestations.
Brad T Tinkle   +2 more
exaly   +3 more sources

Echocardiographic findings in classical and hypermobile Ehlers–Danlos syndromes

American Journal of Medical Genetics Part A, 2005
AbstractStructural cardiovascular alterations in the classical and hypermobile forms of Ehlers–Danlos syndrome(EDS) warrant investigation. We have examined a cohort of 38 patients with hypermobile and classical EDSs using two‐dimensional echocardiography. The cohort includes 7 males and 31 females, with an age range from 12–60 years.
Nazli B, McDonnell   +7 more
openaire   +2 more sources

The Many Facets of Hypermobile Ehlers-Danlos Syndrome

Journal of Osteopathic Medicine, 2020
Abstract Of the 13 subtypes of Ehlers-Danlos Syndromes (EDSs) identified in the 2017 international classification of EDSs, 12 have a recognized, associated genetic mutation. However, hypermobile EDS (hEDS) currently has no identifiable associated gene.
openaire   +2 more sources

Cardiac involvement in classical or hypermobile Ehlers–Danlos syndrome is uncommon

Genetics in Medicine, 2020
Cardiac-valvular and vascular Ehlers-Danlos syndrome (EDS) have significant cardiovascular issues. The prevalence and significance of such abnormalities in classical (cEDS) or hypermobile EDS (hEDS) remain unclear. We report the prevalence of cardiac abnormalities in patients with cEDS and hEDS.We identified 532 pediatric patients with potential EDS ...
Sharon L. Paige   +3 more
openaire   +2 more sources

Orthopaedic Manifestations in Hypermobile Ehlers-Danlos Syndrome

Journal of Bone and Joint Surgery
Background: Hypermobile Ehlers-Danlos syndrome (hEDS) is a collagen disorder affecting multiple organ systems, including the musculoskeletal system. We sought to determine the type and severity of orthopaedic manifestations experienced by these patients.
Josef K. Eichinger   +9 more
openaire   +2 more sources

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