[PDF][PDF] Osler–Weber–Rendu syndrome

JAM Morphet - CMAJ, 2006 - Can Med Assoc
The attached image (Fig. 1) is intended to complement the pulmonary radiography and CT
imaging that accompany the report of a case of hereditary hemorrhagic telangiectasia …

[PDF][PDF] Osler-Weber-Rendu syndrome: A case report with familial clustering

S Grover, RS Grewal, R Verma, H Sahni… - Indian Journal of …, 2009 - ijdvl.com
Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a
rare autosomal dominant disorder manifested by telangiectases of the skin and mucous …

Osler–Weber–Rendu syndrome

BI Mani, AR Rubel, WA Chauhdary… - … Journal of Medicine, 2020 - academic.oup.com
A 57-year-old man with diabetes and chronic hepatitis B presented with epistaxis and
symptomatic anaemia. His past medical history was relevant for recurrent presentations with …

[HTML][HTML] Osler-Weber-Rendu syndrome in relation to dermatology

TL Orizaga-Y-Quiroga, A Villarreal-Martínez… - Actas Dermo …, 2019 - Elsevier
Abstract Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic
telangiectasia, is a rare autosomal dominant disorder with an estimated worldwide …

[PDF][PDF] Osler–Weber–Rendu syndrome

MU Butt, E Yoo, U Khan - QJm, 2016 - academia.edu
Osler–Weber–Rendu syndrome, also known as Hereditary Hemorrhagic Telangiectasia
(HHT), is an autosomal dominant disorder. Telangiectasias and Arterio-Venous …

Life-threatening hemoptysis: case of Osler–Weber–Rendu Syndrome

R Alicea-Guevara, M Cruz Caliz… - Oxford Medical Case …, 2018 - academic.oup.com
Hereditary haemorrhagic telangiectasia (HHT), also known as Osler–Weber–Rendu
syndrome, is a rare autosomal dominant vascular disorder. Patients with HHT may present …

[HTML][HTML] Osler-Weber-Rendu disease: A rare cause of recurrent hemoptysis

AM Khoja, RK Jalan, DL Jain, OV Kajale - Lung India, 2016 - journals.lww.com
Abstract Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia,
is a rare autosomal dominant condition causing systemic fibrovascular dysplasia. It has an …

Unilateral facial telangiectases suggest type 1 segmental manifestation of Osler-Rendu-Weber syndrome in an 11-year-old boy.

P Poblete-Gutiérrez, A Rübben, HF Merk… - European Journal of …, 2003 - europepmc.org
An 11-year-old boy revealed multiple telangiectases confined to the left cheek and the left
side of the lips. Additionally, unilateral epistaxis was present. Radiological examinations of …

Hereditary HaemorrhagicTelangiectasia--A Rare Cause of Severe Anaemia.

P Deshpande, S Bhat, A Karmarkar - The Journal of the Association …, 2014 - europepmc.org
Hereditary Haemorrhagic Telangiectasia also known as Osler-Rendu-Weber disease is a
rare autosomal dominant disorder affecting small vessels of skin and mucosa, usually …

[HTML][HTML] A case of hereditary hemorrhagic telangiectasia

HE Lee, C Sagong, KY Yeo, JY Ko, JS Kim… - Annals of …, 2009 - ncbi.nlm.nih.gov
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 …