Results 101 to 110 of about 5,408,332 (199)

Osler-Weber-Rendu Syndrome - Dental Implications [PDF]

open access: yes, 2009
Osler-Weber-Rendu syndrome (OWRS) is a rare hereditary, autosomal dominant disease characterized by a local angiodysplasia. Its clinical characteristics are vascular hamartomas of the skin and oral mucosa, arteriovenous malformations in the lungs, liver,
MAGALHAES, Marina Helena   +2 more
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Presentation of a rendu-osler-weber patient to emergency department

open access: yes, 2008
Rendu-Osler-Weber disease (hereditary hemorrhagic telangiectasia) is an autosomal dominant familial angiogenesis disorder which presents with the clinical consequences of vascular malformations in mucocutaneous tissues, visceral organs and central ...
Serinken, M, Turkcuer, I, Erdur, B
core  

A case report of recurrent acute ischemic strokes in a young patient with Rendu-Osler-Weber disease [PDF]

open access: yes, 2018
Rendu-Osler-Weber disease is a rare inherited disease of the vasculature, characterized by the development of multiple telangiectasias of the skin and mucous membranes, as well as hemorrhagic syndrome of various localization.
Sidorovich, E. K.   +11 more
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A Case of Osler-Weber-Rendu Syndrome Complicated with Nasal Septum Perforation [PDF]

open access: yes, 2020
Objectives: Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) is a rare autosomal dominant disorder characterized by multiple mucocutaneous telangiectasias and visceral arteriovenous malformations.
Jukhai, Layala   +4 more
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Arterial anastomosis in liver transplantation for Rendu-Osler-Weber disease: two case reports

open access: yes, 2013
Liver transplantation (LT) in patients with hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber, disease is a problematic procedure. In patients with hepatic involvement due to clinically significant arterovenous malformations, there is ...
G. Nita   +9 more
core   +1 more source

Osler-Weber-Rendu Disease with Cardiac Fibroma: A Case Report

open access: yes, 2004
We describe a 6-year-old female patient who presented with hematemesis. There were pin-pointed, non-pulsatile, multiple telangiectases on her right auricle, back of the right ear, neck and gluteal region.
EROĞLU, Ayşe Güler   +4 more
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Osler-Weber-Rendu Disease

open access: yesAmerican Journal of Roentgenology, 2001
M, Matsuo   +5 more
openaire   +3 more sources

Case Report of Osler-Weber-Rendu Syndrome with Incidentally Detected Ipsilateral Renal Adnexal Agenesis

open access: yes
Osler-Weber-Rendu Syndrome, also known as hereditary hemorrhagic telangiectasia, is an autosomal dominant disease characterized by the presence of vascular telangiectasias in the skin and mucosa.
Tarhan, Mustafa Oktay
core   +1 more source

Osler-Weber-Rendu Disease

open access: yesAsian Medical Journal and Alternative Medicine, 2010
openaire   +2 more sources

Hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease)

open access: yes, 2002
Rendu-Osler-Weber disease, or hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant disorder with incomplete penetrance, characterized by vascular anomalies which may virtually develop in many organs.
GUASTAMACCHIA, Edoardo   +7 more
core  

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