Results 41 to 50 of about 1,710,432 (174)
Pulmonary arteriovenous malformation
Journal of the Belgian Society of Radiology, 2011 A 37-year old patient with Rendu-Osler-Weber syndrome presented to our hospital with hypoxy.
E Janssens +4 more
doaj +1 more source
Osler-Weber-Rendu syndrome [PDF]
Heart, 2005 A 54 year old white woman was admitted with a 10 year history of progressive dyspnoea and exertional hypoxia (oxygen saturation fell from 96% to 77% after …
M C, Bates, A, Almehmi
openaire +2 more sources
Indian Journal of Vascular and Endovascular Surgery, 2023 Hereditary hemorrhagic telangiectasia (HHT) (Osler–Weber–Rendu syndrome) is a rare vascular disorder that usually presents with epistaxis, mucocutaneous telangiectasia, and gastrointestinal bleeding.
Tanya Aggarwal +5 more
doaj +1 more source
Anesthetic Considerations for a Patient With Hereditary Hemorrhagic Telangiectasia (Osler–Weber–Rendu Syndrome) Undergoing a Five-Box Thoracoscopic Maze Procedure for Atrial Fibrillation [PDF]
Journal of Investigative Medicine High Impact Case Reports, 2014 Barbara Rogers
exaly +2 more sources
Cerebrovascular Malformations Associated With Hereditary Hemorrhagic Telangiectasia and HHT-Like Syndromes: A Comparative Overview. [PDF]
Eur J NeurolHereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Palermo M, Sturiale CL.
europepmc +2 more sources
Clinical Dermatology Review, 2021 Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder manifested by telangiectases of the skin and mucous membranes and arteriovenous malformations of various organ systems.
Vidhi S Chandibhamar +3 more
doaj +1 more source
Anais Brasileiros de Dermatologia, 2014 The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions.
Juliana Catucci Boza +3 more
doaj +1 more source
Síndrome de Osler Weber Rendau en adulto mayor [PDF]
, 2022 Objective: To expose the main clinical characteristics to make the diagnosis of Hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu syndrome. Case presentation: We present the case of a 70-year-old patient with a history of repeated epistaxis who ...
Esteban Badillo, Laura Yibeth +4 more
core +1 more source
Massive Hemothorax by Ruptured Arteriovenous Malformation [PDF]
Modern MedicineIntroduction and objectives: Osler Weber Rendu disease is a rare genetic disorder characterized by multiple telangiectasias and arteriovenous malformations involving parenchymatous organs, leading to hemorrhagic, sometimes life threatening vascular ...
Genoveva CADAR, Otilia RADU
doaj +1 more source
Pulmonary arteriovenous malformationsm and follow-up imagings
The Pan African Medical Journal, 2020 An 85-year-old caucasian female with past medical history of hypertension, hyperlipidemia, polymyalgia rheumatica, coronary artery disease, Osler-Weber-Rendu syndrome (diagnosed 18 years ago), intermittent epistaxis and pulmonary arteriovenous ...
Pahnwat Tonya Taweesedt, Salim Surani
doaj +1 more source