Results 31 to 40 of about 177,116 (201)

Telangiectasia hemorrágica hereditária: uma causa rara de anemia grave Hereditary hemorrhagic telangiectasia: a rare cause of severe anemia

Jornal Brasileiro de Pneumologia, 2007
Telangiectasia hemorrágica hereditária é uma doença autossômica dominante na qual comunicações arteriovenosas afetam comumente pele, superfícies mucosas, pulmões, cérebro e trato gastrointestinal.
José Wellington Alves dos Santos, Tiago Chagas Dalcin, Kelly Ribeiro Neves, Keli Cristina Mann, Gustavo Luis Nunes Pretto, Alessandra Naimaier Bertolazi   +5 more
doaj   +1 more source

Hereditary hemorrhagic telangiectasia [PDF]

Canadian Medical Association Journal, 2009
Hereditary hemorrhagic telangiectasia, or Osler–Weber–Rendu syndrome, is an autosomal dominant vascular disorder that affects multiple systems. It is characterized by skin and mucosal telangiectasias and arteriovenous malformations. In 1876, Sir John Legg described a case of “hemophilia”
openaire   +2 more sources

Hereditary Hemorrhagic Telangiectasia: Diagnosis and Management

, 2022
Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber syndrome, is a dominantly inheritable rare disease with a prevalence of 1:5000–10,000 inhabitants [...
Cuesta M. Angel, Angel Cuesta, Angel, Cuesta M.   +2 more
core   +1 more source

Mobile Mitral and Aortic Valvular Masses in Patients With Hereditary Hemorrhagic Telangiectasia Receiving Intravenous Bevacizumab

Mayo Clinic Proceedings: Innovations, Quality & Outcomes, 2020
Bevacizumab is now an emerging treatment option for severe hereditary hemorrhagic telangiectasia–related bleeding including epistaxis and gastrointestinal tract bleeding.
Hasan Ahmad Albitar, MD, Yahya Almodallal, MBBS, Rick Nishimura, MD, Vivek N. Iyer, MD, MPH   +3 more
doaj   +1 more source

Low-dose bevacizumab did not reduce epistaxis in patient with hereditary hemorrhagic telangiectasia : a case report [PDF]

, 2020
A 74-year-old man with refractory epistaxis and melena was diagnosed with hereditary hemorrhagic telangiectasia （HHT）. Frequent epistaxis required gauze packing, electrocautery, and blood transfusion. Ileocecal resection did not reduce melena. To control
Ogawa, Hiroshi, Yamauchi, Tomohiko, Tsunoda, Saburo, Yokoyama, Shuji, Utano, Kenichi   +4 more
core  

Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood [PDF]

, 2005
BACKGROUND: Pulmonary arterial hypertension (PAH) is a potentially fatal vasculopathy that can develop at any age. Adult-onset disease has previously been associated with mutations in BMPR2 and ALK-1.
Haworth, SG, Berger, R; id_orcid, Aldred, M A, Morrell, NW, Harrison, RE, Morrell, Nicholas W., Morrell, N W, Mache, CJ, Haworth, S G, Trembath, R C, Mache, Christoph J., Aldred, MA, Trembath, RC, Berger, Rolf, Aldred, Micheala A., Berger, R, Tulloh, R, Harrison, R E, Harrison, Rachel E., Haworth, Sheila G., Mache, C J, Trembath, Richard C., Tulloh, Robert   +22 more
core   +1 more source

Safety of antithrombotic therapy in hereditary hemorrhagic telangiectasia: results from a prospective cohort study

Research and Practice in Thrombosis and Haemostasis
Background: Hereditary hemorrhagic telangiectasia (HHT) is a vascular disorder characterized by a predominant bleeding phenotype. However, patients are also at risk of thrombotic events and may require antithrombotic therapy (AT), for which safety data ...
Luigi Di Martino, Fabiana Agostini, Daniela Feliciani, Barbara Funaro, Annarita Barberio, Rosa Talerico, Antonio Gasbarrini, Roberto Pola, Eleonora Gaetani   +8 more
doaj   +1 more source

Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reports

BMC Neurology, 2011
Background Paradoxical embolism due to pulmonary arteriovenous malformations is the main mechanism of brain infarction in patients with hereditary hemorrhagic telangiectasia.
Viader Fausto, Babin Emmanuel, Cogez Julien, Ribeiro Espartaco, Defer Gilles   +4 more
doaj   +1 more source

Malformações arteriovenosas pulmonares – Associação a telangiectasia hemorrágica hereditária. Casos clínicos e rastreio familiar

Revista Portuguesa de Pneumologia, 2006
Resumo: As malformações arteriovenosas pulmonares são raras e mais de metade dos casos surgem em associação a telangiectasia hemorrágica hereditária.Faz-se uma revisão teórica sobre a apresentação clínica, abordagem diagnóstica, terapêutica
Diva Ferreira, Joana Amado, Raquel Duarte, José Almeida, Paulo Morgado, Teresa Shiang   +5 more
doaj   +1 more source

RENDU-OSLER-WEBER DISEASE AT 75 YEARS OLD WOMAN

Архивъ внутренней медицины, 2017
The publication presents a clinical case of hereditary hemorrhagic telangiectasia in a woman of 75 years. In the first part of the article, literature data on the incidence and features of Rundu-Osler-Weber disease are presented, modern diagnostic ...
A. S. Barmenova, T. A. Bayesheva, N. S. Umbetalina, V. A. Suhova   +3 more
doaj   +1 more source