Results 11 to 20 of about 21,378 (292)

Hereditary hemorrhagic telangiectasia associated with inherited thrombophilia [PDF]

open access: yesVojnosanitetski Pregled, 2017
Introduction. Hereditary hemorrhagic telangiectasia and inherited thrombophilia are genetic disorders with quite opposite clinical manifestation. The main characteristic for hereditary hemorrhagic telangiectasia is recurrent bleeding, while the ...
Roganović Branka   +3 more
doaj   +2 more sources

Splenic Involvement in Hereditary Hemorrhagic Telangiectasia

open access: yesCase Reports in Medicine, 2016
A 33-year-old man who presented with prolonged epigastric pain was referred to our hospital. He had experienced recurrent epistaxis and had a family history of hereditary hemorrhagic telangiectasia.
Susumu Takamatsu   +5 more
doaj   +2 more sources

Genetic Diagnosis of Hereditary Hemorrhagic Telangiectasia: Four Novel Pathogenic Variations in Turkish Patients

open access: yesBalkan Medical Journal, 2020
Aims:Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder characterized by telangiectasia, epistaxis, and vascular malformations. Pathogenic mutations were found in ENG, AVCRL1, SMAD4, and GDF genes.
Mehmet Baysal   +8 more
doaj   +2 more sources

A Case of Hereditary Hemorrhagic Telangiectasia [PDF]

open access: yesAnnals of Dermatology, 2009
Hereditary hemorrhagic telangiectasia, also known as Osler-Weber-Rendu disease, is an autosomal dominant disorder of the fibrovascular tissue. It is characterized by the classic triad of mucocutaneous telangiectasias, recurrent hemorrhages, and familial occurrence.
Ha Eun, Lee   +5 more
openaire   +3 more sources

Hereditary hemorrhagic telangiectasia, embolization, and Young’s procedure: oral surgical management

open access: yesJournal of Oral Medicine and Oral Surgery, 2018
Hereditary hemorrhagic telangiectasia (HHT) case with history of embolization and Young’s procedure: surgical management. Introduction: Osler–Weber–Rendu disease hereditary hemorrhagic telangiectasia (HHT) is a genetic vascular dysplasia.
Malthiery Eve   +5 more
doaj   +2 more sources

The Lung in Hereditary Hemorrhagic Telangiectasia [PDF]

open access: yesRespiration, 2017
Hereditary hemorrhagic telangiectasia (HHT) is a dominantly inherited genetic vascular disorder with an estimated prevalence of 1 in 6,000, characterized by recurrent epistaxis, cutaneous telangiectasia, and arteriovenous malformations (AVMs) that affect many organs including the lungs, gastrointestinal tract, liver, and brain.
Sophie Dupuis-Girod   +2 more
openaire   +5 more sources

10th International Hereditary Hemorrhagic Telangiectasia Scientific Conference, 12-15 June, 2013 - Cork, Ireland

open access: yesHematology Reports, 2013
Book of Abstracts - 10th International Hereditary Hemorrhagic Telangiectasia Scientific Conference, 12-15 June, 2013 - Cork ...
Guest Editors: Carmelo Bernabeu, Luisa M. Botella, Adrian Brady, Marie Faughnan, Urban Geisthoff
doaj   +2 more sources

9th International Hereditary Hemorrhagic Telangiectasia Scientific Conference, 20-24 May 2011 Kemer, Antalya – Turkey

open access: yesHematology Reports, 2011
Book of Abstracts - 9th International Hereditary Hemorrhagic Telangiectasia Scientific Conference, 20-24 May 2011 Kemer, Antalya ...
Guest Editor: Kevin Whitehead, USA
doaj   +2 more sources

Hereditary hemorrhagic telangiectasia with liver cirrhosis: a case report

open access: yesBMC Gastroenterology, 2021
Background Hereditary hemorrhagic telangiectasia is an autosomal dominant hereditary hemorrhagic disease. Its main feature is an abnormal structure of the blood vessel wall.
Linxia Xu   +3 more
doaj   +1 more source

Liver cirrhosis in a patient with hepatic hereditary hemorrhagic telangiectasia and Budd–Chiari syndrome: a case report

open access: yesBMC Gastroenterology, 2020
Background Hereditary hemorrhagic telangiectasia (HHT) often involves the liver, and belongs to abnormal blood vessel disease. The etiology of Budd–Chiari syndrome (BCS) is not clear, but congenital vascular dysplasia is considered to be one of the ...
Bai-Guo Xu   +3 more
doaj   +1 more source

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