Results 1 to 10 of about 5,408,332 (199)

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

Lung India, 2016
Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant condition causing systemic fibrovascular dysplasia. It has an incidence of 1-2/100,000. Phenotypic variation is extreme ranging from asymptomatic
Amir M Khoja, Rahul K Jalan, Dheeraj L Jain, Omkar V Kajale   +3 more
doaj   +5 more sources

Osler-Weber-Rendu Disease Uncovered by Preeclampsia in a Case Report [PDF]

Case Reports in Obstetrics and Gynecology, 2020
Osler-Weber-Rendu disease (OWRD), called hereditary hemorrhagic telangiectasia, is an uncommon genetic illness with the dominant autosomal transmission.
Jamal Ouachaou, Hamza Mimouni, Mohammed Maarad, Yassine Mellagui, Asmae Oulad Amar, Houssam Bkiyar, Imane Kamaoui, Brahim Housni   +7 more
doaj   +6 more sources

Ischemic cholangitis: Lethal complication of Osler-Weber-Rendu disease [PDF]

Radiology Case Reports
Osler-Weber-Rendu disease (OWRD), also known as hereditary haemorrhagic telangiectasia (HHT), is an autosomal dominant genetic disorder characterised by arteriovenous malformations in several organs.
Ouiam Elmqaddem, Hajar Koulali, Abdelkrim Zazour, Meryem Nasiri, Moulay Zahi Ismaili, Ghizlane Kharrasse   +5 more
doaj   +5 more sources

Pulmonary arteriovenous malformation revealing Osler‐Weber‐Rendu disease: A case report [PDF]

Clinical Case Reports, 2022
Osler‐Weber‐Rendu disease is a genetic disease characterized by mucocutaneous and visceral telangiectasias. Pulmonary arteriovenous malformation is one of the main visceral complications revealing Osler‐Weber‐Rendu disease. The present case was a 34‐year‐
Herveat Ramanandafy, Finaritra Princy Parfait Andriamahenina, Michel Harison Tiaray, Anjara Mihaja Nandimbiniaina, Angela Zamelina Razafindrasoa, Sonia Razafimpihanina, Diamondra Andriarimanga, Jean Noêl Solohery Ratsimbazafy, Jocelyn Robert Rakotomizao, Joëlson Lovaniaina Rakotoson, Hanta Marie Danielle Vololontiana   +10 more
doaj   +3 more sources

Osteomalacia Following Iron Infusion Therapy in a Patient With Rendu‐Osler‐Weber Syndrome: F‐18‐FDG PET/CT Discrimination of a Stress Fracture in the Setting of a Musculoskeletal Tumor Mimic [PDF]

Clinical Case Reports
This case report highlights a rare occurrence of osteomalacia induced by hypophosphatemia secondary to ferric carboxymaltose (FCM) therapy in a patient with hereditary hemorrhagic telangiectasia (HHT, or Rendu‐Osler‐Weber syndrome).
Ioannis S. Vasios, Pipitsa N. Valsamaki, Konstantinos Tilkeridis, Savvas Deftereos, Efthymios Iliopoulos   +4 more
doaj   +3 more sources

Rare manifestations in a case of Osler-Weber-Rendu disease. [PDF]

BMJ Case Rep, 2015
Osler-Weber-Rendu disease (OWRD) is a rare vascular dysplasia that presents most commonly with epistaxis. The most dreaded complication, however, is an intracranial haemorrhage. We present a patient with two rare manifestations of OWRD, subdural haematoma and portal venous hypertension, both seldom reported in the literature.
Singh A, Suri V, Jain S, Varma S.
europepmc   +4 more sources

Osler-Weber-Rendu (OWR) Disease and Heart Failure [PDF]

Clinical Medicine Insights: Cardiology, 2009
OWR is a genetic disease, transmitted as an autosomal dominant disorder characterized by arteriovenous malformations predominantly involving the mucocutaneous epithelium.
Arnon Blum, Rafea Shalabi
doaj   +3 more sources

Osler-Weber-Rendu Disease: Unexpected Cause of Anemia. [PDF]

Intern Med, 2023
Kobayashi T, Ishiyama S, Ono Y.
europepmc   +3 more sources

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

A case report of Osler-Weber-Rendu disease with multisystem involvemen

Якутский медицинский журнал
Hereditary hemorrhagic telangiectasia (Osler-Rendu-Weber disease) is a rare disorder with an autosomal dominant inheritance pattern, characterized by small arteriovenous malformations (AVMs) on the mucous membranes and skin (telangiectasias), as well as ...
N. V. Enenkov, A. O. Enenkova, A. G. Yakubovskaya   +2 more
doaj   +2 more sources