Results 91 to 100 of about 1,081,004 (187)
Longitudinal echocardiography in pediatric patients with hypermobile Ehlers‐Danlos syndrome
American Journal of Medical Genetics Part AAbstractVascular Ehlers‐Danlos, Marfan and Loeys‐Dietz syndromes have increased risk of aortic dilation and dissection. Previous early studies showed hypermobile Ehlers‐Danlos syndrome (hEDS) may also have increased risk, with echocardiography screening recommended; subsequent studies have not confirmed the risk or recommended echocardiography.
Hannah, Lahey +3 more
openaire +2 more sources
A Caregiver's Perspective: Identifying “Zebras”—Listening to Patients is a Clinical Necessity
Journal of Patient ExperienceThis caregiver perspective article shares a decades-long experience of a family navigating the health system to obtain an accurate diagnosis for their nonbinary child, ultimately identified with Hypermobile Ehlers-Danlos Syndrome (hEDS) with Median ...
Gil Bashe
doaj +1 more source
Journal of Pain Research, 2022 Kiley C Whalen, Wilson Crone Center for Physician Assistant Studies, Albany Medical College, Albany, NY, USACorrespondence: Wilson Crone, Center for Physician Assistant Studies, Albany Medical College, MC-4, 47 New Scotland Avenue, Albany, NY, 12208, USA,
Whalen KC, Crone W
doaj
Journal of Patient ExperienceAutistic individuals with hypermobile Ehlers-Danlos syndrome (hEDS) often face unique challenges navigating healthcare systems due to lack of clinician awareness, diagnostic delays, misdiagnoses, and systemic barriers.
Sarah Clark
doaj +1 more source
Background: Hypermobile type Ehlers-Danlos Syndrome (hEDS) is subtype of Ehlers-Danlos Syndrome that is a genetic connective tissue disorder with complexities involving joint hypermobility, tissue fragility and severe pain.
Breazeale, Julianna L
core +1 more source
Long COVID and hypermobility spectrum disorders have shared pathophysiology
Frontiers in NeurologyHypermobility spectrum disorders (HSD) and hypermobile Ehlers–Danlos syndrome (hEDS) are the most common joint hypermobility conditions encountered by physicians, with hypermobile and classical EDS accounting for >90% of all cases.
Ravindra Ganesh, Bala Munipalli
doaj +1 more source
, 2021 Summary: • Ehlers Danlos Syndrome (EDS) o Inherited collagen disorder o Different collagen mutations produce the various types o Type I - Gravis form o Type II - Mitis form o Type III - Hypermobile form > Patient have hypermobility of their joints o Type
Andrew G. Lee, MD; Chelsea Livingston
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The Physical and Psychological Impacts of Exercise on hypermobile Ehlers-Danlos Syndrome: A Case Study [PDF]
Hypermobile Ehlers-Danlos Syndrome (hEDS) is a subtype of a series of connective tissue disorders identified by joint hypermobility and multisystemic symptoms.
Posey, Savannah
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Ehlers-Danlos syndrome with soft-tissue contractures
, 1992 We report four patients with a form of Ehlers-Danlos syndrome associated with soft-tissue contractures from birth and skin hyperalgesia. In early infancy, these cases were thought to be forms of arthrogryposis multiplex congenita, Larsen's syndrome or ...
S Oshita +4 more
core +1 more source
Diagnostic Methods for Hypermobile Ehlers-Danlos Syndrome: A Scoping Review
This research project consists of a scoping review aimed at mapping and synthesizing the scientific evidence on the diagnostic methods used for Hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorders (HSD). Ehlers-Danlos Syndromes (
Stéfani Sousa Borges +3 more
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