Results 31 to 40 of about 1,710,432 (184)

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

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

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

, 2009
Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder manifested by telangiectases of the skin and mucous membranes and arteriovenous malformations of various organ systems.
Sahni, H., Grewal, R.S., Verma, Rajesh, Grover, Sanjiv, Sinha, Preema, Muralidhar, R.   +5 more
core   +2 more sources

Epistaxis Runs in the Family

Oman Medical Journal, 2021
A 36-year-old male presented with multiple red spots over the tongue that appeared at the age of 10 years. In the past two decades, he had suffered from recurrent spontaneous episodes of profuse bleeding from the nose and tongue lesions, requiring ...
Abheek Sil, Dibyendu Bikash Bhanja, Sayantani Chakraborty   +2 more
doaj   +1 more source

Pulmonary arteriovenous malformation

Journal of the Belgian Society of Radiology, 2011
A 37-year old patient with Rendu-Osler-Weber syndrome presented to our hospital with hypoxy.
E Janssens, P Leyman, T De Beule, L Ardies, P D’haenens   +4 more
doaj   +1 more source

Case report of hereditary hemorrhagic telangiectasia with pulmonary and hepatic arteriovenous malformations

Indian Journal of Vascular and Endovascular Surgery, 2023
Hereditary hemorrhagic telangiectasia (HHT) (Osler–Weber–Rendu syndrome) is a rare vascular disorder that usually presents with epistaxis, mucocutaneous telangiectasia, and gastrointestinal bleeding.
Tanya Aggarwal, Neerja Meena, Shivani Ramnani, Jai Chowdhary, Nikhil Bansal, Rahul Bhargava   +5 more
doaj   +1 more source

A female with mucocutaneous telangiectases and portal hypertension: A case report of osler-weber-rendu syndrome

Clinical Dermatology Review, 2021
Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder manifested by telangiectases of the skin and mucous membranes and arteriovenous malformations of various organ systems.
Vidhi S Chandibhamar, Bhagirath R Patel, Ani Patel, Jignaben K Padhiyar   +3 more
doaj   +1 more source

Left extended hepatectomy with biliary resection and reconstruction for hilar cholangiocarcinoma in patient with Osler-Rendu-Weber disease: a case report and review of literature. [PDF]

Updates Surg
: Osler-Rendu-Weber syndrome is a genetic disease that involves organs, liver included, characterized by alterations in the vessel walls, making them more vulnerable to spontaneous rupture and bleeding indeed.
Marchese A, Conci S, Pecori S, Castelli C, Contro A, Mansueto G, Scarpa A, Ruzzenente A.   +7 more
europepmc   +2 more sources

Case for diagnosis [PDF]

Anais Brasileiros de Dermatologia, 2014
The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions.
Juliana Catucci Boza, Timotio Volnei Dorn, Fabiana Bazanella de Oliveira, Renato Marchiori Bakos   +3 more
doaj   +1 more source

Fibrodysplastic implications for transvenous embolization of a high-flow pelvic arteriovenous malformation in Osler-Weber-Rendu syndrome [PDF]

, 2015
Osler-Weber-Rendu syndrome is a rare genetic disorder that commonly features high-flow arteriovenous malformations (AVM) within the pulmonary, intracranial, and visceral circulation.
Nassiri, Naiem, Rahimi, Saum, Thomas, Jones   +2 more
core   +1 more source