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Hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease)
The Lancet, 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
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 2008Rendu-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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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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Multiple Cerebral Angiomas and Rendu-Osler-Weber Disease: Case Report
Neurosurgery, 1991Abstract A 25-year-old man was hospitalized after suffering a subarachnoid hemorrhage. Arteriograms disclosed two arteriovenous malformations, one of which was asymptomatic. Rendu-Osler-Weber disease was suspected because of the concomitant existence of cutaneous telangiectases, Review of the literature shows that in 12 previously ...
B, Aesch +3 more
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Hereditary Hemorrhagic Telangiectasia (Rendu–Osler–Weber Disease)
2004Rendu-Osler-Weber disease, or hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant disorder with incomplete penetrance, characterized by vascular anomalies which may virtually develop in many organs. The prevalence varies and may range from 1/3,500 to 1/5,000 in specific regions.
Carlo Sabbà +2 more
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ROTH SPOTS IN A RENDU–OSLER–WEBER SYNDROME
RETINAL Cases & Brief ReportsPurpose: 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 +4 more
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[Syndromes 14. Rendu-Osler-Weber disease].
Nederlands tijdschrift voor tandheelkunde, 2002The Rendu-Osler-Weber disease is due to an autosomal dominant disease with multiple telangiectasia in skin and mucosa. Recurrent bleeding of the nose is due to telangiectasia of the nasal mucosa. Haemorrhage of the oral mucosa also occurs. Extensive arteriovenous malformations can be present in lungs, liver and brain. Treatment of bleedings in the oral
J A, Baart, J M, van Hagen
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43 Congreso de la Sociedad Española de Endoscopia Digestiva (Libro de Comunicaciones), 2021
María Ortiz de Solórzano +8 more
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María Ortiz de Solórzano +8 more
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