Results 141 to 150 of about 1,710,432 (174)

Hereditary Hemorrhagic telangiectasia: a rare familial case with delayed diagnosis despite decades of recurrent bleeding. [PDF]

Oxf Med Case Reports
Rahi AV, Kumar A, Singh J, Kumar N, Kumar K, Dinkar A.   +5 more
europepmc   +1 more source

Hereditary hemorrhagic telangiectasia in a 72-year-old woman presenting with recurrent epistaxis and liver cirrhosis: a case report. [PDF]

Ann Med Surg (Lond)
Jha R, Subedi P, Sinha A, Shah S.
europepmc   +1 more source

Familial Hereditary Hemorrhagic Telangiectasia with Stroke in Two Generations: Diagnostic Delay and the Role of Patient-Specific Three-Dimensional-Printed Models in Endovascular Planning. [PDF]

Acta Cardiol Sin
Chao KY, Chen CY, Chu YZ, Lîm HK, Mu SC, Chien YH.   +5 more
europepmc   +1 more source

From Epistaxis to Embolization: A Case of Hereditary Hemorrhagic Telangiectasia Presenting With Spontaneous Hemothorax. [PDF]

Cureus
Kathiresan V, Thangakunam B.
europepmc   +1 more source

Osler-Weber-Rendu Syndrome—Pathological Manifestations and Autopsy Considerations

Journal of Forensic Sciences, 2001
Abstract An 18-year-old university student with Osler-Weber-Rendu disease collapsed in the bathroom. Attempted resuscitation was unsuccessful. Her past history included recurrent epistaxes, mucosal telangiectasias, intracranial arteriovenous malformations with previous hemorrhage, a single pulmonary arteriovenous malformation, recent ...
Byard, R., Schliebs, J., Koszyca, B.
openaire   +4 more sources

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Telangiectasias in Osler‐Weber‐Rendu Syndrome

Otolaryngology - Head and Neck Surgery, 2017
Jason Cohn
exaly   +3 more sources

Osler-Weber-Rendu syndrome--dental implications. [PDF]

Journal (Canadian Dental Association), 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, kidney and brain, and episodes of epistaxis.
Paulo Sérgio, da Silva Santos, Karin Sá, Fernandes, Marina Helena, Magalhães   +2 more
openaire   +2 more sources

Rendu-Osler-Weber Syndrome: case report and literature review [PDF]

Brazilian Journal of Otorhinolaryngology, 2008
SummaryHereditary Hemorrhagic Telangiectasia or Rendu-Osler-Weber Disease is a rare fibrovascular dysplasia that makes vascular walls vulnerable to trauma and rupture, causing skin and mucosa bleeding.
Alfredo Rafael Dell'Aringa
exaly   +2 more sources

Osler–Weber–Rendu syndrome simulating pulmonary metastasis

Postgraduate Medical Journal, 2013
Osler–Weber–Rendu syndrome, also known as hereditary haemorrhagic telangiectasia (HHT), is an autosomal dominant disorder of abnormal blood vessel formation manifesting as telangiectasias and arteriovenous malformations (AVMs). The criteria for the diagnosis of HHT are epistaxis, multiple telangiectasias at mucocutaneous surfaces, AVMs in larger organ ...
Jorge Luiz, Pereira E Silva, Gláucia, Zanetti, Edson, Marchiori   +2 more
openaire   +2 more sources