The Turkish Journal of Pediatrics, 2001 In most instances, congenital arteriovenous fistula is only one manifestation of a more widespread abnormality; 60% of patients also have hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber syndrome).
R Olguntürk +5 more
doaj +4 more sources
Enfermedad de Rendu-Osler-Weber Rendu-Osler-Weber syndrome
Revista Cubana de Medicina, 2009 La telangiectasia hemorrágica hereditaria o enfermedad de Rendu-Osler-Weber es autosómica dominante, se caracteriza por la presencia de múltiples telangiectasias en piel y mucosas asociadas a malformaciones arteriovenosas de distintos órganos.
Gloria Astencio Rodríguez +5 more
doaj +1 more source
Life-threatening hemoptysis: case of Osler-Weber-Rendu Syndrome. [PDF]
Oxf Med Case Reports, 2018 Hereditary haemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is a rare autosomal dominant vascular disorder. Patients with HHT may present with a wide spectrum of clinical manifestations, some considered to be life-threatening. We present the case of a 53-year-old male who presented with massive haemoptysis.
Alicea-Guevara R +8 more
europepmc +4 more sources
Osler-Weber-Rendu Syndrome as a Rare Cause of Liver Cirrhosis. [PDF]
CureusIt is essential to comprehend the clinical manifestations of hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome. This autosomal dominant vascular disorder presents with distinct symptoms, including mucocutaneous telangiectasia, epistaxis, gastrointestinal bleeding, and iron deficiency anemia.
Tuna C +5 more
europepmc +3 more sources
Osler-Weber-Rendu Syndrome in Relation to Dermatology
Actas Dermo-sifiliográficas, 2019 Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder with an estimated worldwide prevalence of 1 case per 10,000 population. Its clinical manifestations are the result of arteriovenous malformations characterized by telangiectases that can affect the skin, mucous membranes, and solid ...
J Ocampo-Candiani
exaly +3 more sources
Osler-Weber-Rendu syndrome: a rare cause of iron deficiency. [PDF]
J Gen Intern Med, 2011 A 52-year-old man with frequent epistaxis presented with fatigue and exertional dyspnea. On physical examination, multiple telangiectasias were noted on the patient’s face, lips, tongue (Fig. 1), and finger tips (Fig. 2). Laboratory analysis demonstrated iron deficiency anemia (hemoglobin, 8.2 g/dl; ferritin: 15 ng/ml).
Ozkok A, Akpinar TS, Akkaya V.
europepmc +4 more sources
Case report: Diagnosis of hereditary hemorrhagic telangiectasia (Osler Weber Rendu Syndrome) in a 23-year-old male presented with anemia and thrombocytopenia and its response to bevacizumab [PDF]
Frontiers in Medicine, 2022 Said Amin
exaly +2 more sources
PREGNANCY AND HERITABLE CONNECTIVE TISSUE DISORDERS (MARFAN SYNDROME, EHLERS DANLOS SYNDROME, OSLER-WEBER-RENDU DISEASE) [PDF]
Акушерство, гинекология и репродукция, 2016 The article describes some inherited disorders (Marfan syndrome, Ehlers-Danlos syndrome, Osler-Weber-Rendu disease) that affects the connective tissue with prominent manifestations in the skeletal, ocular, and cardiovascular systems during the pregnancy.
L. S. Radetskaya
doaj +2 more sources
Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu syndrome). [PDF]
J Gen Intern Med, 2017 Santos MA.
europepmc +4 more sources
Pulmonary arterovenous malformation causing hemothorax in a pregnant woman without Osler- Weber-Rendu syndrome [PDF]
Open Medicine (Poland), 2015 Pio Zeppa +2 more
exaly +2 more sources