Results 11 to 20 of about 1,555,246 (206)

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
core   +5 more sources

Spontaneous Coronary Artery Dissection as Presenting Feature of Vascular Ehlers-Danlos Syndrome [PDF]

Cardiogenetics, 2021
A spontaneous coronary artery dissection as the sole presenting feature of vascular Ehlers-Danlos syndrome is an uncommon finding. We present a 33-year-old woman with sudden onset chest pain caused by a spontaneous coronary artery dissection.
J. Bos, E. Overwater, M.T. Dirksen, S. Simsek, S. Demirdas, A.C. Houweling   +5 more
doaj   +2 more sources

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   +2 more sources

Vascular-type Ehlers-Danlos syndrome caused by a hitherto unknown genetic mutation: a case report

Journal of Medical Case Reports, 2013
Introduction Vascular-type Ehlers-Danlos syndrome is an autosomal dominant disease that causes arterial spurting, intestinal perforation, uterine rupture and hemopneumothorax due to decreased production of type III collagen.
Kashizaki Fumihiro, Hatamochi Atsushi, Kamiya Kazunori, Yoshizu Akira, Okamoto Hiroaki   +4 more
doaj   +2 more sources

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

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   +2 more sources

Late conversion after endovascular abdominal aortic aneurysm repair in a patient with Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques, 2019
Vascular Ehlers-Danlos syndrome is associated with life-threatening events. The management of the disease is challenging because of the emergency presentation of symptoms and the tissue friability of the aorta.
Georgios Karaolanis, MD, MSc, PhD, Özgun Sensebat, MD, Giovanni Torsello, MD, Theodosios Bisdas, MD, Konstantinos P. Donas, MD   +4 more
doaj   +2 more sources

Celiprolol Treatment in Patients with Vascular Ehlers-Danlos Syndrome [PDF]

European Journal of Vascular and Endovascular Surgery, 2019
Vascular Ehlers-Danlos syndrome (vEDS) is a rare monogenetic disease caused by pathogenic variants in procollagen 3A1. Arterial rupture is the most serious clinical manifestation. A randomised controlled trial, the Beta-Blockers in Ehlers-Danlos Syndrome Treatment (BBEST) trial, reported a significant protective effect of the beta blocker celiprolol ...
Hassan Baderkhan, Anders Wanhainen, Anna Stenborg, Eva-Lena Stattin, Martin Björck   +4 more
openaire   +5 more sources

Ehlers-Danlos syndrome type IV

Orphanet Journal of Rare Diseases, 2007
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous ...
Germain Dominique P
doaj   +2 more sources

Vascular type Ehlers‐Danlos syndrome with intra‐abdominal hemorrhage due to ruptured hepatic aneurysm: A case report

Acute Medicine & Surgery
Background Vascular Ehlers‐Danlos syndrome has a high mortality rate due to hemorrhagic complications. Case Presentation We report a case of vascular‐type Ehlers‐Danlos syndrome diagnosed due to rupture of multiple celiac aneurysms.
Masaou Tanaka, Kentaro Ueda, Takafumi Yonemitsu, Shinobu Tamura, Akira Ikoma, Tetsuo Sonomura, Shigeaki Inoue   +6 more
doaj   +2 more sources

Ehlers–Danlos Syndrome: Not Just Joint Hypermobility

Case Reports in Medicine, 2018
Ehlers–Danlos syndrome is an umbrella term for a group of heritable soft connective tissue disorders which is characterized by joint hypermobility, skin texture and elasticity abnormalities, and visceral and vascular fragility or dysfunctions.
Tina Bregant, Milica Klopcic Spevak
doaj   +2 more sources