Results 51 to 60 of about 1,172,427 (185)

Pregnancy outcome in joint hypermobility syndrome and Ehlers–Danlos syndrome

, 2017
IntroductionAn increased risk of preterm birth in women with joint hypermobility syndrome or Ehlers-Danlos syndrome is suspected. Material and methodsIn this nationwide cohort study from 1997 through 2011, women with either joint hypermobility syndrome ...
Jonas F. Ludvigsson, Sundelin, Heléne,, Olof Stephansson, Stephansson, Olof,, Johansson, Kari,, Ludvigsson, Jonas F.,, Heléne E. K. Sundelin, Kari Johansson, Sundelin, Helene E. K.,   +8 more
core   +1 more source

Suspected Mitochondrial Dysfunction and Complex Pathophysiology in Fatal Hypermobile Ehlers–Danlos Syndrome: Insights from a Case Report and Post-Mortem Findings

Biomedicines
Background/Objectives: Hypermobile Ehlers–Danlos Syndrome (hEDS) is a complex connective tissue disorder with multi-systemic manifestations that significantly impact quality of life.
Arash Shirvani, Purusha Shirvani, Ugochukwu Jonah, Brian E. Moore, Michael F. Holick   +4 more
doaj   +1 more source

The prevalence of hypermobile Ehlers–Danlos syndrome at a gender-affirming primary care clinic

SAGE Open Medicine
Objective: This study utilized a sample of trangender, nonbinary, and gender-diverse (TGD) patients to build on emerging literature that suggests that hypermobile Ehlers–Danlos syndrome may be overrepresented in TGD populations.
Theo Stein, Shannon Collins, Joshua St. Louis   +2 more
doaj   +1 more source

Ehlers-Danlos syndrome with infective endocarditis: A case report with literature review

IDCases, 2019
We report a patient with Ehlers-Danlos syndrome and mitral valve infective endocarditis. The case was complicated due to multiorgan involvement and initially diagnosed as hand-foot-and-mouth disease.
Yang Jiao, Mark S. Rasnake, Michael T. McCormack, J. Francis Turner   +3 more
doaj   +1 more source

Spontaneous compartment syndrome and endovascular repair of tibioperoneal trunk pseudoaneurysm in Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques, 2021
Vascular Ehlers-Danlos syndrome is caused by mutations in the COL3A1 (collagen type III alpha-1) gene, resulting in loss of integrity of arteries and hollow organs. Patients are predisposed to dissection, aneurysm, and organ rupture.
Krystina N. Choinski, MD, Nicole Ilonzo, MD, Rami O. Tadros, MD, Jeffrey W. Olin, DO, John Phair, MD   +4 more
doaj   +1 more source

Investigating the Relationship Between Sensory Processing, Pain and Toe Walking Gait: A Survey Study

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Aim This study aimed to examine sensory processing patterns, the frequency and impact of parent‐reported pain in children who toe walk across a range of diagnoses using validated caregiver‐report tools. Methods An online cross‐sectional survey was distributed internationally between July 2024 and March 2025.
Jack H. Donne, Verity Pacey, Desiree Polt, Jennifer A. Powell, Michael C. Fahey, Cylie M. Williams   +5 more
wiley   +1 more source

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, Yun-Hee Lim, Jung Sun Park, Sang Seok Lee, Kye-Min Kim   +4 more
doaj   +1 more source

Oral Manifestations of Non Vascular Ehlers‐Danlos Syndrome Cross‐Sectional Study

Oral Diseases, EarlyView.
ABSTRACT Background Ehlers–Danlos syndromes are rare hereditary connective tissue disorders; however, their oral manifestations remain poorly characterized in molecularly confirmed individuals. The aim of this study was to describe the oral phenotype of patients with non‐vascular Ehlers‐Danlos syndromes compared to healthy controls.
Aude Grand, Benjamin P. J. Fournier, Grégoire Chevalier, Karelle Benistan, François Côme Ferré   +4 more
wiley   +1 more source

Classical Ehlers-Danlos syndrome: etiology, presentation and management. Literature review. [PDF]

, 2021
Ehlers-Danlos syndrome is a rare genetic condition classified into 13 subtypes based on clinical presentation, genetic mutation type and inheritance pattern.
Berankytė, Ieva,, Balsytė, Ignė,
core  

Using the suture/adhesive strips combination technique for skin closure in an individual with Ehlers–Danlos Syndrome

JPRAS Open, 2019
Combining sutures with adhesive strips to avoid the ‘cheese-wiring’ effect in individuals with fragile skin is a method that has been described previously. Here we demonstrate its application in an individual with Ehlers-Danlos Syndrome. Keywords: Cheese-
S. Shaharan, J.C.Y. Chan, T. Bage, J. Kelly   +3 more
doaj   +1 more source