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

E.C. te Veldhuis; A.H. te Veldhuis; F.S. van Dijk; M.L. Kwee; J.M. van Hagen; J.A. Baart; I. van der Waal

doi:https://doi.org/10.1016/j.tripleo.2007.08.017

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

E.C. te Veldhuis, A.H. te Veldhuis, F.S. van Dijk, M.L. Kwee, J.M. van Hagen, J.A. Baart, I. van der Waal

Research output: Contribution to journal › Article › Academic › peer-review

27 Citations (Scopus)

Abstract

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 the lips, oral cavity, fingers, and nose, and visceral arteriovenous malformations. Timely recognition of this syndrome makes screening for complications, preventive measurements, and genetic counselling possible. The important role of the dental profession in the recognition of this genetic disease is emphasized. In addition, a brief overview of the current literature is presented.

Original language	Undefined/Unknown
Pages (from-to)	e38-e41
Journal	Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology
Volume	105
Issue number	2
DOIs	https://doi.org/10.1016/j.tripleo.2007.08.017
Publication status	Published - 2008

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https://doi.org/10.1016/j.tripleo.2007.08.017

https://pure.uva.nl/ws/files/4128109/59686_292438.pdf

Cite this

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title = "Rendu-Osler-Weber disease: update of medical and dental considerations",

abstract = "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 the lips, oral cavity, fingers, and nose, and visceral arteriovenous malformations. Timely recognition of this syndrome makes screening for complications, preventive measurements, and genetic counselling possible. The important role of the dental profession in the recognition of this genetic disease is emphasized. In addition, a brief overview of the current literature is presented.",

author = "{te Veldhuis}, E.C. and {te Veldhuis}, A.H. and {van Dijk}, F.S. and M.L. Kwee and {van Hagen}, J.M. and J.A. Baart and {van der Waal}, I.",

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AU - te Veldhuis, E.C.

AU - te Veldhuis, A.H.

AU - van Dijk, F.S.

AU - Kwee, M.L.

AU - van Hagen, J.M.

AU - Baart, J.A.

AU - van der Waal, I.

PY - 2008

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AB - 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 the lips, oral cavity, fingers, and nose, and visceral arteriovenous malformations. Timely recognition of this syndrome makes screening for complications, preventive measurements, and genetic counselling possible. The important role of the dental profession in the recognition of this genetic disease is emphasized. In addition, a brief overview of the current literature is presented.

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