Results 11 to 20 of about 11,601 (222)

Vascular Ehlers‐Danlos syndrome and pregnancy: A systematic review

BJOG: an International Journal of Obstetrics and Gynaecology
(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 ...
Jean Gondry, Arthur Foulon
exaly   +3 more sources

Twin pregnancy with untyped Ehlers-Danlos syndrome requiring prompt genetic testing: A case report

Case Reports in Women's Health, 2022
Ehlers-Danlos syndrome is a rare genetic disorder that presents with a variety of pathologies depending on the disease type. Among them, vascular Ehlers-Danlos syndrome requires extremely careful management as there have been many reports of fatal ...
Shiori Ogawa, Tasuku Mariya, Yuya Fujibe, Marie Ogawa, Keiko Ikeda, Miyako Mizukami, Yoshika Kuno, Aki Ishikawa, Shinichi Ishioka, Akihiro Sakurai, Tsuyoshi Saito   +10 more
doaj   +1 more source

Pediatric Innominate Artery Pseudoaneurysm Rupture in Vascular Ehlers-Danlos Syndrome: A Case Report

Clinical Practice and Cases in Emergency Medicine, 2021
Introduction: Ehlers-Danlos syndrome is a well classified connective tissue disorder recognized by its features of hyperextensibility of joints and hyperelasticity of the skin.
Aimee Vos, Katharine M. Burns
doaj   +1 more source

Adults with Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome: A cross-sectional study of life satisfaction

Journal of Rehabilitation Medicine, 2021
Objective: To explore life satisfaction among adults with Loeys-Dietz and those with vascular Ehlers-Danlos syndrome. Design: Postal survey in 2018. Participants and methods: Persons with molecularly verified Loeys-Dietz syndrome or vascular Ehlers ...
Heidi Johansen, Gry Velvin, Kerstin Fugl-Meyer, Ingeborg Beate Lidal   +3 more
doaj   +1 more source

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

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   +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

Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome [PDF]

, 2013
Background: Whereas mutations affecting the helical domain of type I procollagen classically cause Osteogenesis Imperfecta (OI), helical mutations near the amino (N)-proteinase cleavage site have been suggested to result in a mixed OI/Ehlers-Danlos ...
De Paepe, Anne, Goemans, Nathalie, Gyftodimou, Yolanda, Holmberg, Eva, Lopez-Gonzalez, Vanesa, Malfait, Fransiska, Mortier, Geert, Nampoothiri, Sheela, Petersen, Michael Bjorn, Symoens, Sofie   +9 more
core   +4 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

Repeated intestinal perforations in vascular Ehlers-Danlos syndrome: a case report of a novel mutation in the COL3A1 gene

Surgical Case Reports, 2023
Background Ehlers-Danlos syndrome is an inherited connective-tissue disorder characterized by skin hyperextensibility, joint hypermobility, and tissue fragility.
Taichi Horino, Yuji Miyamoto, Mayuko Ohuchi, Katsuhiro Ogawa, Naoya Yoshida, Takatoshi Ishiko, Chieko Kukinaka, Rumi Sasaki, Takashi Ohba, Hideo Baba   +9 more
doaj   +1 more source

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