Rendu-Osler-Weber disease: update of medical and dental considerations
| Autor: | A.H. te Veldhuis, F.S. van Dijk, E.C. te Veldhuis, I. van der Waal, M.L. Kwee, J.M. van Hagen, J.A. Baart |
|---|---|
| Přispěvatelé: | Human genetics, Oral and Maxillofacial Surgery / Oral Pathology, CCA - Disease profiling, University of Groningen, MKA (OUD, ACTA) |
| Rok vydání: | 2008 |
| Předmět: |
Male
medicine.medical_specialty Activin Receptors Type II Genetic counseling Receptors Cell Surface Disease PHENOTYPE Oral cavity Tongue Diseases MECHANISMS SDG 3 - Good Health and Well-being PULMONARY ARTERIOVENOUS-MALFORMATIONS Antigens CD medicine Humans HEREDITARY HEMORRHAGIC TELANGIECTASIA Telangiectasia General Dentistry Nose Genes Dominant Smad4 Protein MUTATIONS business.industry Endoglin Lip Diseases Middle Aged SERIES ANTIGENS CD medicine.disease Dermatology Rendu-Osler-Weber disease GENOTYPE Surgery ENG MANIFESTATIONS medicine.anatomical_structure Otorhinolaryngology Tongue disease Mutation Female Telangiectasia Hereditary Hemorrhagic Oral Surgery medicine.symptom business CEREBRAL ABSCESS |
| Zdroj: | Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology, 105(2), e38-e41 Oral surgery oral medicine oral pathology oral radiology and endodontology, 105(2), E38-E41 Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology, 105(2), e38-e41. Wiley-Blackwell Publishing Ltd Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology, 105(2), e38-e41. Mosby Inc. 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 2008, ' Rendu-Osler-Weber disease: update of medical and dental considerations ', Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology, vol. 105, no. 2, pp. e38-e41 . https://doi.org/10.1016/j.tripleo.2007.08.017 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 2008, ' Rendu-Osler-Weber disease: update of medical and dental considerations ', Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology, vol. 105, no. 2, pp. e38-e41 . https://doi.org/10.1016/j.tripleo.2007.08.017 |
| ISSN: | 1079-2104 1528-395X |
| DOI: | 10.1016/j.tripleo.2007.08.017 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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