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Rendu-Osler-Weber: γονότυπος και φαινότυπος

, 2014
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Hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease)

Lancet, The, 2003
Correspondence 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 ...
Shuichi Kaneko
exaly   +3 more sources

Rendu-Osler-Weber disease: update of medical and dental considerations

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 2008
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., te Veldhuis, A.H., van Dijk, F.S., Kwee, M.L., van Hagen, J.M., Baart, J.A., van der Waal, I.   +6 more
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Rendu-Osler-Weber syndrome

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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Hereditary Hemorrhagic Telangiectasis (Rendu-Osler-Weber Disease)

Optometry and Vision Science, 1981
Abstract 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, 1996
We 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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ROTH SPOTS IN A RENDU–OSLER–WEBER SYNDROME

RETINAL Cases & Brief Reports
Purpose: The purpose of this study was to describe the molecular diagnosis and atypical ocular presentation of a patient who suffered for a Rendu–Osler–Weber syndrome associated with juvenile polyposis syndrome. Methods: This is a case report of a patient who underwent fundus ...
Thomas Ferreira de Moura, Amélie Servettaz, Adrien Henry, Carl Arndt, Alexandre Denoyer   +4 more
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Rendu-Osler-Weber syndrome

Medicina Clínica (English Edition), 2019
Sonia, Benítez-Rivero, Jonathan, Camacho Romero, Daniel, Eiroa   +2 more
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