Results 21 to 30 of about 1,710,432 (184)

Interventional approach to splenic vascular malformation, a rare manifestation of Rendu-Osler-Weber syndrome [PDF]

Radiology Case Reports
Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is an autosomal dominant genetic disorder that interferes with angiogenesis and leads to abnormal vascular development.
Jose Urbano, MD, PhD, Adrian Viteri-Noël, MD, Jorge Cobos-Alonso, MD, Vicente Gómez del Olmo, MD, PhD   +3 more
doaj   +2 more sources

A Rare Case of Upper Gastrointestinal Bleeding: Osler-Weber-Rendu Syndrome

Medicina, 2022
Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia (HHT), is a rare, autosomal dominant condition that affects approximately 1 in 5000 patients causing abnormal blood vessel formation.
Anna Jargielo, Anna Rycyk, Beata Kasztelan-Szczerbinska, Halina Cichoz-Lach   +3 more
doaj   +3 more sources

Overcoming Complexity: Percutaneous Embolization for Hepatic Artery Pseudoaneurysms in Hereditary Hemorrhagic Telangiectasia (HHT) [PDF]

Indian Journal of Radiology and Imaging
Osler-Weber-Rendu syndrome also known as hereditary hemorrhagic telangiectasia (HHT) is a rare vascular dysplasia affecting multiple organ systems in the body.
Anjali Sah, Rajendra Kumar Behera, Anuradha Sharma, Shivanand Gamanagatti, Ayush Agarwal, Soumya Jagannath Mahapatra   +5 more
doaj   +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

Radiological findings in the liver of a patient with Rendu-Osler-Weber syndrome. [PDF]

Radiol Bras, 2019
Rodrigues RA, Rodrigues RA, Freitas VC, de Araujo ALE, Parente DB.   +4 more
europepmc   +5 more sources

Osler-Weber-Rendu Syndrome [PDF]

Indian Dermatology Online Journal
Arpita N. Rout, Deepak K. Sahu, Chandra S. Sirka   +2 more
doaj   +2 more sources

Investigation of cardiovascular characteristics in a patient with hereditary hemorrhagic telangiectasia, a case report. [PDF]

Physiol Rep
Abstract Hereditary Hemorrhagic Telangiectasia (HHT) may present with symptoms arising from multiple organ systems. In this case report, the focus is on cardiovascular manifestations, including total blood volume, cardiac function, and the potential role of the sympathetic nervous system (SNS) in the clinical picture. The commonly held supposition that
Søndergaard S, Madsen S.
europepmc   +2 more sources

Patient with anaemia and Rendu-osler-weber syndrome [PDF]

Revista Andaluza de Patología Digestiva, 2021
Resumen Varón de 66 años con Telangiectasia Hemorrágica Hereditaria tipo I que consulta por astenia intensa detectándose en analítica Hb 4 mg/dl; VCM 100,5%. El paciente no refiere síntomas de sangrado. En gastroscopia se visualizan múltiples malformaciones vasculares de tamaño variable y sin sangrado activo en esófago, estómago, siendo más ...
A Roa Colomo, AM Caballero Mateos, J García Márquez   +2 more
openaire   +1 more source

Hepatic Encephalopathy in Osler-Weber-Rendu Syndrome

Annals of Internal Medicine: Clinical Cases, 2022
Hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu syndrome is a rare condition that leads to multiple vascular malformations. We describe the interesting patient case of a woman with recurrent epistaxis secondary to Osler-Weber-Rendu syndrome ...
Sakthi Gautham, Christopher J. Haas
doaj   +1 more source

Final observation of an extremely severe case of Osler-Weber-Rendu disease in teaching at the pregraduate and postgraduate stages of education and the use of current English-language Internet applications for doctors and patients

Медицина неотложных состояний, 2023
Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome, Osler-Weber-Rendu disease, etc) is diagnosed clinically according to the so called Curacao criteria, if at least three of four of them are present: recurrent spontaneous epistaxis ...
V.M. Rudichenko, N.V. Snigir, V.О. Кrivets   +2 more
doaj   +1 more source