Results 21 to 30 of about 1,915,528 (208)

Vascular Ehlers-Danlos Syndrome and Pregnancy: A Systematic Review

Obstetric Anesthesia Digest
(BJOG. 2024;131:1620-1629. doi: 10.1111/1471-0528.17893) The prevalence of Ehlers-Danlos syndrome (EDS) is ∼1 in 5000, and it is characterized by joint hyperlaxity, high skin elasticity, and fragile connective tissue. There are 13 known subtypes, and the most frequently occurring of these are classic EDS, hypermobile EDS, and vascular EDS ...
Haem, Théo, Benson, Betty, Dernoncourt, Amandine, Gondry, Jean, Schmidt, Jean, Foulon, Arthur   +5 more
openaire   +3 more sources

The vascular type of Ehlers–Danlos syndrome

Анналы клинической и экспериментальной неврологии, 2017
EhlersDanlos syndrome (EDS) type IV (vascular type of EDS)is a rare inherited autosomal dominant connective-tissue disordercaused by a mutation in the procollagen III gene (the COL3A1gene).
Maria V. Gubanova, Larisa A. Dobrynina, Lyudmila A. Kalashnikova   +2 more
doaj   +2 more sources

Genetic testing for vascular Ehlers-Danlos syndrome and other variants with fragility of the middle arteries

The EuroBiotech Journal, 2018
Ehlers-Danlos syndrome (EDS) is an umbrella term for various inherited connective tissue disorders associated with mutations in genes involved in extracellular matrix formation.
Rakhmanov Yeltay, Maltese Paolo Enrico, Bruson Alice, Castori Marco, Beccari Tommaso, Dundar Munis, Bertelli Matteo   +6 more
doaj   +2 more sources

Vertebral Tortuosity Is Associated With Increased Rate of Cardiovascular Events in Vascular Ehlers‐Danlos Syndrome [PDF]

, 2023
Background Arterial tortuosity is associated with adverse events in Marfan and Loeys-Dietz syndromes but remains understudied in Vascular Ehlers-Danlos syndrome.
Siddharth K. Prakash, Nicholas Dodd, Li, Jesse, Dianna M. Milewicz, Stephens, Sara B, Shalhub, Sherene, Beecroft, Taylor, Devereux, Richard B, Kalyan Kancherla, Asch, Federico M, Michael Huang, Reed E. Pyeritz, Sara B. Stephens, Shaine A. Morris, Shohet, Ralph V, Peter Byers, Teniola Shittu, Jesse Li, Eagle, Kim, Lacro, Ronald V, Holmes, Kathryn W, Seitaro Oda, Cecchi, Alana, Ralph V. Shohet, Pyeritz, Reed E, Sherene Shalhub, Roman, Mary J, Rajesh Krishnamurthy, Weigand, Justin D, Kim Eagle, Ronald V. Lacro, Oda, Seitaro, Milewicz, Dianna M, Alana Cecchi, Prakash, Siddharth K, Byers, Peter, Kancherla, Kalyan, Preiss, Liliana, Federico M. Asch, Krishnamurthy, Rajesh, Shittu, Teniola, Kathryn W. Holmes, Justin D. Weigand, Scott A. LeMaire, LeMaire, Scott A, Morris, Shaine A, Dodd, Nicholas, Doan, Tam T, Tam T. Doan, Liliana Preiss, Taylor Beecroft, Richard B. Devereux, Mary J. Roman, Huang, Michael   +53 more
core   +1 more source

Vascular Ehlers‐Danlos Syndrome

Journal of Pediatric Gastroenterology and Nutrition, 2018
Clinical History Image Findings Discussion Find Diagnosis Differential ...
Boutaina, Zemrani, Elizabeth, McLeod, Elizabeth, Rogers, Joanna, Lawrence, Debi, Feldman, Victoria, Evans, Helen, Shalley, Julie, Bines   +7 more
  +6 more sources

Vascular Ehlers Danlos syndrome [PDF]

Circulation: Cardiovascular Genetics, 2014
Vascular Ehlers–Danlos syndrome (vEDS) is an autosomal dominant disease that affects the arteries, bowels, uterus, and skin. Affected individuals can have spontaneous rupture of hollow organs, such as the bowels or gravid uterus, along with arterial dissections and ruptures that lead to premature death.
Yuranga Weerakkody, Francis Fortin, Bruno Di Muzio   +2 more
openaire   +3 more sources

Vascular Ehlers-Danlos syndrome [PDF]

Journal of Cardiology, 2009
Vascular type Ehlers-Danlos syndrome (EDS) is a rare inherited disease with an autosomal dominant trait. The mutation of the COL3A1 gene which encodes type III collagen, is responsible of early vascular (spontaneous arterial rupture or dissection), digestive (perforation) and obstetrical events (uterine and arterial rupture).
Nakamura, Michinari, Yajima, Junji, Oikawa, Yuji, Ogasawara, Ken, Uejima, Tokuhisa, Abe, Keiko, Aizawa, Tadanori   +6 more
openaire   +3 more sources

Clinical periodontal diagnosis

Periodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi, Andrea Roccuzzo, Jean‐Claude Imber, Alexandra Stähli, Björn Klinge, Niklaus P. Lang   +5 more
wiley   +1 more source

Operative repair of right intrathoracic subclavian artery aneurysms in patients with genetic arteriopathy

Journal of Vascular Surgery Cases and Innovative Techniques, 2023
True intrathoracic subclavian artery aneurysms (SCAAs) are rare and have various etiologies. Right intrathoracic SCAAs pose specific anatomic challenges to repair.
Bryce L. French, MD, Anthony M. Menghini, MS, Christopher R. Burke, MD, Peter H. Byers, MD, Sherene Shalhub, MD, MPH, FACS DFSVS   +4 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