Results 61 to 70 of about 1,081,004 (187)

Long‐term outcomes in patients with postural orthostatic tachycardia syndrome with an average follow‐up of over 20 years

Journal of Internal Medicine, Volume 300, Issue 3, Page 299-311, September 2026.
Abstract Background Postural orthostatic tachycardia syndrome (POTS) is a chronic form of orthostatic intolerance that primarily affects female patients. There are scarce data evaluating the long‐term outcomes in POTS. Objectives This study sought to evaluate the long‐term impacts of POTS over multiple decades in adult patients.
Kate M. Bourne, Alfredo Gamboa, Bonnie Black, Juliette Hall, Italo Biaggioni, Cyndya A. Shibao, André Diedrich, Amanda Peltier, Giris Jacob, Luis Okamoto, Robert S. Sheldon, Satish R. Raj   +11 more
wiley   +1 more source

Developing a self-management intervention to manage hypermobility spectrum disorders (HSD) and hypermobile Ehlers-Danlos syndrome (hEDS): An analysis informed by behaviour change theory [PDF]

, 2021
Purpose: Hypermobility Spectrum Disorders (HSD) and Hypermobile Ehlers-Danlos Syndrome (hEDS) are heritable connective tissue disorders associated with joint instability and pain, but with scant guidance for supporting patients.
Palmer, Shea, Walsh, Nicola E., Moss, Timothy, Bennett, Sarah E., Walsh, Nicola, Moss, Tim, Bennett, Sarah   +6 more
core   +1 more source

Arthroscopic Anterior and Posterior Glenohumeral Capsular Augmentation With Gracilis Allograft

Arthroscopy Techniques, Volume 15, Issue 7, July 2026.
Abstract Multidirectional instability in patients with connective tissue disorders such as Ehlers‐Danlos syndrome (EDS) is difficult to treat due to poor tissue quality and frequent failure of standard repairs. We describe an arthroscopic technique using gracilis tendon allografts to perform an anterior and posterior capsular augmentation in the ...
Michael D. Maloney, Omkar N. Prabhavalkar, Samantha Levin, Richard Lander, Brett P. Salazar, Sandeep Mannava   +5 more
wiley   +1 more source

Hypermobile Ehlers-Danlos Syndrome (hEDS) [PDF]

, 2019
Ehlers-Danlos Syndrome is a genetic connective tissue disease with varying expressions and phenotypes. Hypermobile Ehlers-Danlos Syndrome (hEDS) is the most prevalent subgroup within this disease category.
Akers, Jocelyn
core  

Generalized Joint Hypermobility in Adolescent Idiopathic Scoliosis: Greater Curve Flexibility, Larger Thoracic Kyphosis, but Higher Complication Risk

Orthopaedic Surgery, Volume 18, Issue 7, Page 1414-1425, July 2026.
Generalized joint hypermobility in adolescent idiopathic scoliosis is linked to greater spinal flexibility and increased thoracic kyphosis, but also elevates the risk of surgical complications, despite no significant differences in patient‐reported outcomes.
Di Liu, Kexin Xu, Xiangjie Yin, Terry Jianguo Zhang, Nan Wu, on behalf of the Deciphering Disorders Involving Scoliosis and Comorbidities study   +5 more
wiley   +1 more source

Surgical management of pes planus in children with hypermobile Ehlers-Danlos: A case report and review of literature

Foot & Ankle Surgery: Techniques, Reports & Cases
Ehlers-Danlos Syndrome (EDS) is a genetic condition that affects your body's connective tissues. There are many subtypes to the disease, the most relevant to the lower extremity is hypermobile EDS.
Aaron Abraham, DPM, Robert Brarens, DPM, FACFAS   +1 more
doaj   +1 more source

Prevalence and quality of temporomandibular disorders, chronic pain and psychological distress in patients with classical and hypermobile Ehlers-Danlos syndrome: an exploratory study

Orphanet Journal of Rare Diseases, 2023
Background The Ehlers-Danlos syndromes are a group of clinically and genetically heterogeneous hereditary diseases affecting the connective tissue. They are characterized by hypermobility of the joints, hyperextensible skin and friable tissue.
Leon Willich, Lauren Bohner, Jeanette Köppe, Jochen Jackowski, Marcel Hanisch, Ole Oelerich   +5 more
doaj   +1 more source

Children and adolescents with disorders of gut–brain interaction with comorbid hypermobility and orthostatic intolerance have worse outcomes

Journal of Pediatric Gastroenterology and Nutrition, Volume 82, Issue 6, Page 1394-1399, June 2026.
Abstract Objectives Disorders of gut–brain interaction (DGBI) affect about 40% of children and are often comorbid with hypermobility spectrum disorders (HSDs) and orthostatic intolerance (OI). However, how these comorbidities impact outcomes in pediatric DGBI is not well understood.
Neha Santucci, Austin VonAxelson, Jesse Li, Kahleb Graham, Jennifer Hardy, Megan Miller, Rashmi Sahay   +6 more
wiley   +1 more source

Parents' Experiences of Children's Healthcare for Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders [PDF]

, 2022
Hypermobile Ehlers-Danlos syndrome (hEDS) and hypermobility spectrum disorders (HSD) are underdiagnosed hereditary connective tissue disorders requiring health care across specialties.
Bell, Lauren; id_orcid, Pearce, Gemma; id_orcid   +1 more
core   +1 more source

Beighton Scoring System Use in Generalized Joint Hypermobility Studies Has Greater Scientific Rigor Than Joint‐Specific or Arthroscopy Joint Hypermobility Studies

Arthroscopy, Sports Medicine, and Rehabilitation, Volume 8, Issue 2, April 2026.
Purpose To compare the scientific rigor of Beighton Scoring System (BSS) use in generalized joint hypermobility (JH) studies (healthy subject injury risk/rate, physiological or kinesiological function determination) and joint‐specific or arthroscopy JH studies; to identify the most commonly used BSS score thresholds; and to describe ways to improve BSS
John Nyland, Essa Gul, Jonathon Lewis, Justin Givens, Ryan Krupp, Jarod Richards   +5 more
wiley   +1 more source