Results 31 to 40 of about 583,024 (194)

Pulmonary arteriovenous fistula in the newborn: a case report of Rendu-Osler-Weber syndrome and a review of the literature

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, D Oğuz, S Tunaoğlu, C Ikizler, A Sezgin, S Kula   +5 more
doaj   +3 more sources

Osteomalacia Following Iron Infusion Therapy in a Patient With Rendu-Osler-Weber Syndrome: F-18-FDG PET/CT Discrimination of a Stress Fracture in the Setting of a Musculoskeletal Tumor Mimic. [PDF]

Clin Case Rep
ABSTRACT This case report highlights a rare occurrence of osteomalacia induced by hypophosphatemia secondary to ferric carboxymaltose (FCM) therapy in a patient with hereditary hemorrhagic telangiectasia (HHT, or Rendu‐Osler‐Weber syndrome). A 21‐year‐old man presented with left tibial pain without prior trauma, accompanied by severe hypophosphatemia ...
Vasios IS, Valsamaki PN, Tilkeridis K, Deftereos S, Iliopoulos E.   +4 more
europepmc   +2 more sources

Rendu-Osler-weber disease. Case report [PDF]

, 2016
Rendu-Osler-Weber disease is the most frequently observed genetic hemorrhagic angiopathy with local wall thinning, distention of microcirculation vessels' lumen, and incomplete local hemostasis. This pathology is inherited per autosomal-dominant type with a various pathologic gene's frequency of occurrence.
Kurochkin S., Chuvashaev I., Zidikhanov D., Gafurov M.   +3 more
openaire   +4 more sources

Life-threatening anaemia in patient with hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome) [PDF]

Open Medicine (Poland), 2020
Melánia Mikołajczyk-Solińska, Jacek Kasznicki   +1 more
exaly   +2 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

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

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

Epistaxis e Hemorragia Digestiva Recorrente: Manifestação da Síndrome Osler-Weber-Rendu

Gazeta Médica, 2020
A telangiectasia hemorrágica hereditária ou síndrome Osler-Weber-Rendu é uma doença vascular hereditária autossómica dominante, que se apresenta, geralmente, com telangiectasias mucocutâneas, epistaxe, hemorragia gastrointestinal, anemia ferripriva e ...
Marisa Isabel de Sousa Ferreira Rosete, Margarida Gaudêncio, Susana Magalhães, Fernando Ferraz e Sousa, Amélia Pereira   +4 more
doaj   +1 more source

Syndrome in Question [PDF]

Anais Brasileiros de Dermatologia, 2014
Rendu-Osler-Weber Syndrome also known as Hereditary Hemorrhagic Telangiectasia is a rare systemic fibrovascular dysplasia, with dominant autosomal inheritance.
Sheila Itamara Ferreira do Couto Meireles, Sônia Maria Fonseca de Andrade, Maria Fernanda Gomes, Fernanda Aalmeida Nunes Castro, Antonio José Tebcherani   +4 more
doaj   +1 more source