Zobrazeno 1 - 10
of 261
pro vyhledávání: '"hypermobile Ehlers–Danlos syndrome"'
Autor:
Stephanie L. Grach, Daniel V. Dudenkov, Beth Pollack, DeLisa Fairweather, Chris A. Aakre, Bala Munipalli, Ivana T. Croghan, Michael R. Mueller, Joshua D. Overgaard, Katelyn A. Bruno, Nerissa M. Collins, Zhuo Li, Ryan T. Hurt, Michal C. Tal, Ravindra Ganesh, Dacre T. R. Knight
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundMany patients experience persistent symptoms after COVID-19, a syndrome referred to as Long COVID (LC). The goal of this study was to identify novel new or worsening comorbidities self-reported in patients with LC.MethodsPatients diagnosed
Externí odkaz:
https://doaj.org/article/abf6d26f995f4f5ca958aece3d09bf51
Autor:
Ravindra Ganesh, Bala Munipalli
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Hypermobility 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. Hypermobility ha
Externí odkaz:
https://doaj.org/article/435d055736404de0bb5c8d2f8f0af23b
Publikováno v:
Journal of Pain Research, Vol Volume 17, Pp 1273-1284 (2024)
Norman J Marcus,1,2 Lexi Robbins,1 Aya Araki,1 Edward J Gracely,3,4 Theoharis C Theoharides5,6 1Norman Marcus Pain Institute, New York, NY, USA; 2Department of Anesthesiology and Neurological Surgery, Weill Cornell Medicine, New York, NY, USA; 3Famil
Externí odkaz:
https://doaj.org/article/7a87d43a0abe462a9b018486418e8f1f
Autor:
Michail Panagiotopoulos, Maria Tsiriva, Lito Vogiatzi-Vokotopoulou, Konstantinos Koukoumpanis, Nikolaos Kathopoulis, Athanasios Douligeris, Athanasios Protopapas, Lina Michala
Publikováno v:
Case Reports in Women's Health, Vol 44, Iss , Pp e00661- (2024)
Hypermobile Ehlers-Danlos syndrome (hEDS) is the most common type of EDS, characterized by joint hypermobility, frequent dislocations, and chronic pain. Genetic markers are not typically used in diagnosis.A 17-year-old clinically diagnosed with hEDS
Externí odkaz:
https://doaj.org/article/00d6015958e9419d8990e0b8cf50708b
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
The Ehlers-Danlos Syndromes (EDS) represent a group of hereditary connective tissue disorders, with the hypermobile subtype (hEDS) being the most prevalent. hEDS manifests with a diverse array of clinical symptoms and associated comorbidities spannin
Externí odkaz:
https://doaj.org/article/386cf8a1f17c4d01bb52e3baf15921fb
Publikováno v:
Frontiers in Rehabilitation Sciences, Vol 5 (2024)
BackgroundEhlers–Danlos syndrome (EDS) is a common group of inherited connective tissue disorders with a prevalence as high as 0.75%–2% of the population. Physical manifestations include pain and decreased proprioception, especially in more mobil
Externí odkaz:
https://doaj.org/article/b9736d5a1fad4514bc58fa762ab6d77a
Autor:
Aurore Fernandez, Manon Jaquet, Bérengère Aubry‐Rozier, Marc Suter, Selma Aybek, Chantal Berna
Publikováno v:
Brain and Behavior, Vol 14, Iss 2, Pp n/a-n/a (2024)
Abstract Background The hypermobile Ehlers–Danlos syndrome (hEDS) and hypermobility spectrum disorders (HSD) are connective tissue disorders characterized by generalized joint hypermobility, associated with chronic pain and several symptoms, such a
Externí odkaz:
https://doaj.org/article/67ac35bf618c47329352a50968e129cd
Publikováno v:
Clinical Case Reports, Vol 12, Iss 1, Pp n/a-n/a (2024)
Key Clinical Message Omalizumab may be a beneficial adjunct treatment option for hEDS patients require to improve pain control, ability to perform ADLs and functionality and social engagement, and most importantly, quality of life.
Externí odkaz:
https://doaj.org/article/256a71a35e5e4139ada72a97e3428309
Autor:
DeLisa Fairweather, Katelyn A. Bruno, Ashley A. Darakjian, Barbara K. Bruce, Jessica M. Gehin, Archana Kotha, Angita Jain, Zhongwei Peng, David O. Hodge, Todd D. Rozen, Bala Munipalli, Fernando A. Rivera, Pedro A. Malavet, Dacre R. T. Knight
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
BackgroundJoint pain is a common symptom in patients with hypermobile Ehlers-Danlos Syndrome (hEDS), hypermobility spectrum disorders (HSD) and fibromyalgia. The goal of this study was to determine whether symptoms and comorbidities overlap in patien
Externí odkaz:
https://doaj.org/article/9a38cc6f5b624b20a5b7c3be90f83883
Autor:
Haley Gagnon, Claire E. Lunde, Ziyan Wu, Eduardo N. Novais, David Borsook, Christine B. Sieberg
Publikováno v:
Children, Vol 10, Iss 9, p 1562 (2023)
Ehlers–Danlos Syndrome (EDS) is a rare disease affecting the skin, joints, vasculature, and internal organs. Approximately 85% of those affected are categorized as the hypermobile type (hEDS), which is associated with numerous medical and psychiatr
Externí odkaz:
https://doaj.org/article/211d69d0ef61425093541ca43de89f6c