Results 31 to 40 of about 3,078 (199)

Change in gliding properties of the iliotibial tract in hypermobile Ehlers–Danlos Syndrome [PDF]

Journal of Ultrasound, 2023
Abstract Purpose Fascial changes in hypermobile Ehlers–Danlos syndrome (hEDS), a heritable connective tissue disorder, can be used visualized with sonoelastography. The purpose of this study was to explore the inter-fascial gliding characteristics in hEDS.
Tina J. Wang, Antonio Stecco, Robert Schleip, Carla Stecco, Carmelo Pirri   +4 more
openaire   +3 more sources

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, J. Elliott, Craig Munns, Verity Pacey, David O Sillence   +4 more
doaj   +3 more sources

Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome

Balkan Medical Journal, 2019
Efforts on recognition, diagnosis, and management of the presumed, most common connective tissue disorder hypermobile Ehlers-Danlos syndrome have been an ongoing challenge, even decades after the description of this condition.
Irman Forghani
doaj   +1 more source

Idiopathic osteoporosis, Ehlers–Danlos syndrome, postural orthostatic tachycardia syndrome, and mast cell activation disorder in a 27‐year‐old male patient: A unique case presentation

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
doaj   +1 more source

A Heterozygous Variant of TGFB3 in a Patient With an Atypical Presentation of Loeys–Dietz Syndrome: A Case Report

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, Meagan N. McNicholas, Christina M. Laukaitis   +2 more
doaj   +1 more source

Neurovisceral phenotypes in the expression of psychiatric symptoms [PDF]

, 2015
This review explores the proposal that vulnerability to psychological symptoms, particularly anxiety, originates in constitutional differences in the control of bodily state, exemplified by a set of conditions that include Joint Hypermobility, Postural ...
Aktas, Al-Rawi, Anderson, Andrew P. Owens, Arunkalaivanan, Baeza-Velasco, Bagai, Bayles, Beacher, Benarroch, Bendik, Benrud-Larson, Birner, Boddaert, Bohora, Bovell, Bulbena, Bulbena, Bulbena, Bulbena, Bulbena, Bulbena, Buodo, Castori, Child, Christopher J. Mathias, Cohen, Critchley, Critchley, Critchley, De Kort, De Wandele, Eccles, Eccles, Eccles, Ekman, Engel, Esler, Esler, Fenton, Friedman, Fu, Ganzeboom, Garcia Campayo, Gazit, Giada, Gracie, Grahame, Grahame, Grubb, Hakim, Hakim, Hugo D. Critchley, Hunt, Jessica A. Eccles, Joyner, Kanjwal, Kapoor, Karaca, Karan, Kaya, Kelly, Khurana, Khurana, Kirby, Koldas Dogan, Kouakam, Lader, Lambert, Lammers, Lee, Leftheriotis, Lemche, Lemche, Lewis, Lewis, Linzer, Lonsdale-Eccles, Low, Luborsky, Mallorqui-Bague, Martin-Santos, Masuki, Mathias, Mathias, Mayer-Gross, McGrady, Milhorat, Mohammed, Morgan, Mulvey, Nicotra, Nijs, Noppen, Ocon, Ocon, Ofluoglu, Ojha, Parsaik, Paulus, Peggs, Phillips, Porges, Pritchard, Raj, Raj, Ramos, Ross, Rozen, Sanches, Satoshi Umeda, Savage, Schievink, Schondorf, Seth, Sierra, Sierra, Sierra, Simeon, Sledge, Smith, Stachenfeld, Stewart, Stoler, Tinkle, Tracey, Umeda, Ventura, Vounotrypidis, Wooley, Yazici, Zarate, Zysko   +132 more
core   +2 more sources

The value of dynamic elastomeric fabric orthoses in the management of a complex hypermobile Ehlers‐Danlos syndrome patient: A case report

Clinical Case Reports, 2023
The use of dynamic elastomeric fabric orthoses is examined in a young woman with hypermobile Ehlers‐Danlos syndrome (hEDS) referred for physiotherapy with hip dysplasia, prior to a right periacetabular osteotomy.
Anna Higo, Gemma Pearce, Shea Palmer, Louise Grant   +3 more
doaj   +1 more source

A novel method of assessing balance and postural sway in patients with hypermobile Ehlers-Danlos syndrome

Frontiers in Medicine, 2023
Patients with hypermobile Ehlers-Danlos syndrome (hEDS) frequently suffer from poor balance and proprioception and are at an increased risk for falls.
Miguel Whitmore, Brittany Barker, Katie Chudej, Ciarra Goines, Jenna Kester, Hannah Campbell, Anna Jeffcoat, Brynn Castleberry, Thomas William Lowder   +8 more
doaj   +1 more source

Association Between Joint Hypermobility Syndrome and Developmental Coordination Disorder – A Review. [PDF]

, 2012
Introduction: The term joint hypermobility syndrome (JHS) was adopted after clinicians became aware of the myriad of symptoms associated with this multisystemic condition.
Clark, Carol J., Khattab, Ahmed D.
core   +1 more source

Outcomes of revisional bariatric surgery in patient with hypermobile Ehlers-Danlos syndrome. [PDF]

J Surg Case Rep
Abstract Ehlers–Danlos syndrome (EDS), a rare group of inherited connective tissue disorders caused by alterations in collagen synthesis, has the potential for disrupted tissue healing leading to morbidity in patients undergoing gastrointestinal surgery.
Friedman A, Eisenberg D.
europepmc   +4 more sources