Hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease)

Lancet

Volumn 362, Issue 9394, 2003, Pages 1490-1494

  Fuchizaki, Uichiro ^a,c   Miyamori, Hirotoshi ^a   Kitagawa, Shunsuke ^a   Kaneko, Shuichi ^b   Kobayashi, Kenichi ^b  

^a Keiju Medical Center   (Japan)

^b KANAZAWA UNIVERSITY   (Japan)

^c Keiju Medical Center   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AGED; ARGON PLASMA COAGULATION; ARTICLE; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC TEST; DISEASE COURSE; FEMALE; HUMAN; LABORATORY TEST; PRIORITY JOURNAL; RENDU OSLER WEBER DISEASE; TREATMENT OUTCOME;

EID: 0242329836     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(03)14696-X     Document Type: Review

References (15)

1. Guttmacher A.E., Marchuk D.A., White R.I. Jr. Hereditary hemorrhagic telangiectasia. N Engl J Med. 333:1995;918-924.
2. Haitjema T., Westermann C.J., Overtoom T.T., et al. Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) new insights in pathogenesis, complications, and treatment. Arch Intern Med. 156:1996;714-719.
3. Hanes F.M. Multiple hereditary telangiectases causes hemorrhage (hereditary hemorrhagic telangiectasia). Bull Johns Hopkins Hosp. 20:1909;63-73.
4. Rendu H. Épistaxis répétées chez un sujet porteur de petits angiomes cutanés et muqueux. Gaz des Hôpitaux 1896: 1322-1323.
5. Osler W. On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes. Bull Johns Hopkins Hosp. 7:1901;333-337.
6. Weber F.P. Multiple hereditary developmental angiomata (telangiectases) of the skin and mucous membranes associated with recurring haemorrhages. Lancet. 2:1907;160-162.
7. Shovlin C.L., Guttmacher A.E., Buscarini E., et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet. 91:2000;66-67.
8. McAllister K.A., Grogg K.M., Johnson D.W., et al. Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nat Genet. 8:1994;345-351.
9. Johnson D.W., Berg J.N., Baldwin M.A., et al. Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. Nat Genet. 13:1996;189-195.
10. Urness L.D., Sorensen L.K., Li D.Y. Arteriovenous malformations in mice lacking activin receptor-like kinase-1. Nat Genet. 26:2000;328-331.
11. Gibbs D.D. Rendu-Osler-Weber disease: a triple eponymous title lives on. J R Soc Med. 79:1986;742-743.
12. Henri Rendu (1844-1902): Rendu-Osler-Weber disease. JAMA 1966; 197: 583.
13. Cushing H. The life of Sir William Osler. 1925;Clarendon Press, Oxford.
14. Bliss M. William Osler: a life in medicine. 1999;Oxford University Press, New York.
15. Hall L.A. A "remarkable collection": the papers of Frederick Parkes Weber FRCP (1863-1962). Med Hist. 45:2001;523-532.