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Hereditary hemorrhagic telangiectasia patient with pulmonary arteriovenous malformation: A case report. [PDF]
Pang CW.
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Rendu-Osler-Weber disease: an unusual presentation.
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Hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease)
Lancet, The, 2003Correspondence to: Dr Uichiro Fuchizaki, Keiju Medical Center, 94 Tomioka-cho, Nanao, Ishikawa 926-8605, Japan (e-mail: fuchi@p1.coralnet.or.jp) Hereditary haemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber disease, is an autosomal dominant disorder characterised by epistaxis, cutaneous telangiectasia (figure 3), and visceral ...
Uichiro, Fuchizaki +4 more
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Rendu-Osler-Weber disease: update of medical and dental considerations
Rendu-Osler-Weber disease, also known as hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant inherited disorder characterized by an aberrant vascular development. The reported prevalence is approximately 1 per 5,000-10,000. The clinical manifestations consist of recurrent spontaneous nosebleeds, telangiectasias characteristically at ...
te Veldhuis, E.C. +6 more
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BMJ, 2014
A 55 year old man presented with recurrent epistaxis and no risk factors or family history. Examination showed extensive telangiectasia on his nasal …
A. Banigo, G. MacDougall
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A 55 year old man presented with recurrent epistaxis and no risk factors or family history. Examination showed extensive telangiectasia on his nasal …
A. Banigo, G. MacDougall
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Hereditary Hemorrhagic Telangiectasis (Rendu-Osler-Weber Disease)
Optometry and Vision Science, 1981Abstract A case of a male patient with hereditary hemorrhagic telangiectasis (Rendu‐Osler‐Weber disease) is described. Discussion includes the natural course and appearance of the lesions and the recommended optometric management.
T T, McMahon, J H, Maino
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Recurrent Massive Hemothorax in Rendu-Osler-Weber Syndrome
Southern Medical Journal, 1996We report a case of Rendu-Osler-Weber syndrome, occurring as sudden death after two episodes of massive hemothorax. Autopsy revealed massive hemothorax resulting from spontaneous rupture of one of three subpleural arteriovenous malformations. Review of the patient's hospital records showed that she had had a massive spontaneous hemothorax 13 years ...
P A, Adegboyega, G, Yuoh, A, Adesokan
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