Results 1 to 10 of about 1,915,478 (171)

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

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   +2 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

Interesting Case of Lung Fibrosis in a Patient With Vascular Ehlers Danlos Syndrome [PDF]

Respirology Case Reports
A 39‐year‐old man with recurrent spontaneous (including bilateral) pneumothoraces and haemoptysis had unusual thoracic computed tomography (CT) abnormalities.
Alicia Su Huey Kwan, Viral Nanda, Taleea Younas, Harshana Bandara   +3 more
doaj   +2 more sources

Percutaneous transhepatic coil embolisation of a common hepatic artery aneurysm in vascular Ehlers–Danlos syndrome [PDF]

CVIR Endovascular
Background Vascular Ehlers–Danlos syndrome is a rare connective tissue disorder characterised by arterial fragility, predisposing patients to life-threatening vascular complications. Endovascular aneurysm management in these individuals poses significant
Oliver Chan, Hariesha Pathmaraj, Chris Grieco, Nadeem Shaida   +3 more
doaj   +2 more sources

A de novo variant of the COL3A1 gene: causality of vascular Ehlers-Danlos syndrome [PDF]

Advances in Laboratory Medicine
To establish diagnosis of vascular Ehlers-Danlos syndrome (VEDS) through genetic testing. This syndrome is characterized by muscle and arterial ruptures and a tendency to easy brusing, thin skin with visible veins and acrogeric facial features that may ...
Gutiérrez Romero Estrella, Padilla Apuntate Nuria, Izquierdo Álvarez Silvia   +2 more
doaj   +2 more sources

Pulmonary Mycobacterium avium complex infection with vascular Ehlers–Danlos syndrome: A case report [PDF]

Respiratory Medicine Case Reports
A female patient developed multiple intestinal perforations at 31 and 43 years of age. Because of her family history of pneumothorax and intestinal perforation, Ehlers–Danlos syndrome (EDS) was suspected when she visited our hospital at 52 years. She was
Ken Okamura, Rintaro Noro, Toru Tanaka, Takeru Kashiwada, Yosuke Tanaka, Yoshinobu Saito, Kazue Fujita, Koichi Akutsu, Tomoko Sahara, Koichiro Kamio, Takeshi Yamada, Kazuo Kasahara, Masahiro Seike   +12 more
doaj   +2 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

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

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

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