Results 21 to 30 of about 411,420 (197)

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   +1 more source

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

Rendu-Osler-Weber Syndrome: A Case Report [PDF]

Macedonian Journal of Medical Sciences, 2014
Hereditary hemorrhagic telangectasia (HHT) or Rendu-Osler-Weber syndrome, is a rare genetic disorder with autosomal dominance and variable penetrance. The typical findings of the disease are telangiectasias in skin and mucous membranes, and arteriovenous malformations presenting in the organs like lung, intestine, brain and liver.
Ignjatović, Vesna, Belić, Branislav, Matović, Milovan, Vukomanović, Vladimir   +3 more
openaire   +3 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

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

Rendu-Osler-Weber Syndrome: case report and literature review [PDF]

Brazilian Journal of Otorhinolaryngology, 2008
Alfredo Rafael Dell'Aringa
exaly   +2 more sources

Cerebrovascular Malformations Associated With Hereditary Hemorrhagic Telangiectasia and HHT-Like Syndromes: A Comparative Overview. [PDF]

Eur J Neurol
Hereditary 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

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