Results 21 to 30 of about 11,601 (222)

Ruptured ulnar artery aneurysm in vascular Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques, 2020
Vascular Ehlers-Danlos syndrome (vEDS), also known as type IV Ehlers-Danlos syndrome, is a rare inherited connective tissue disease that affects 1 in 50,000 to 250,000 individuals.
Ryan Howard, MD, Nicholas Osborne, MD
doaj   +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

Iatrogenic distal aortic rupture in a patient with vascular Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques, 2023
Vascular Ehlers-Danlos syndrome is a rare inherited connective tissue disorder that can result in significant morbidity and mortality. This report details an iatrogenic aortic rupture during an endovascular approach in the management of critical limb ...
Mohammad M. Zagzoog, MD, Sean A. Crawford, MD, Thomas Le Houérou, MD, Antoine Gaudin, MD, Stéphan Haulon, MD, PhD, Dominique Fabre, MD, PhD   +5 more
doaj   +1 more source

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

Hypermobile Ehlers-Danlos Syndrome during Pregnancy, Birth and Beyond: A Review of Midwifery Care Considerations [PDF]

, 2018
The Ehlers-Danlos Syndromes (EDS) are an underdiagnosed group of conditions with implications and risks associated with childbearing. Those with EDS suggest that healthcare professionals have a lack of awareness in this area, and consequently describe ...
Pearce, Gemma, Pezaro, Sally, Reinhold, Emma   +2 more
core   +6 more sources

Rupture of a Median Sacral Artery Aneurysm in a Patient with Vascular Ehlers Danlos Syndrome

EJVES Vascular Forum, 2020
Introduction: Vascular Ehlers Danlos syndrome is a rare connective tissue disease that is associated with various arterial complications. Report: A 25 year old man with vascular Ehlers Danlos syndrome presented with acute lower back pain as a result of a
Merel J. Verhagen, Rutger W. van der Meer, Carla S.P. van Rijswijk, Jan van Schaik   +3 more
doaj   +1 more source

Cardiovascular manifestations of type IV Ehlers-Danlos syndrome – A case report

Revista Portuguesa de Cardiologia, 2022
Type IV Ehlers-Danlos syndrome (vascular) is a rare connective tissue disease caused by COL3A1 gene mutation on type III collagen. Clinical presentation is related to vascular fragility and risk of rupture of the arterial wall.
Tiago Sepúlveda Santos, Rita Marçal, Oana Moldovan, Leonor Carvalho, José Luís Ducla-Soares   +4 more
doaj   +1 more source

Ehlers Danlos Syndrome: An Unusual Presentation You Need to Know about [PDF]

, 2013
The Ehlers Danlos syndromes (EDS) comprise a group of connective tissue disorders characterized by tissue fragility of the skin, ligaments, blood vessels and internal organs.
Karaa, Amel, Stoler, Joan M.
core   +3 more sources

Aortic dissection in a patient with novel frameshift COL5A1 variant of classical Ehlers-Danlos syndrome

European Journal of Case Reports in Internal Medicine, 2023
Classical Ehlers-Danlos syndrome (cEDS) is one of the 13 subtypes of Ehlers-Danlos syndrome, which has the major clinical criteria of hyperextensibility skin, atrophic scars, and generalised joint hypermobility.
Lídia Caley, Ana Campar, Teresa Mendonça, Fátima Farinha   +3 more
doaj   +1 more source