| 释义 |
Rendu–Osler–Weber, n. Med.
Brit. |ˈrɒndju ˌɒslə ˈwɛbə|, |ˈrɛndju ˌɒslə ˈwɛbə|, |ˈrɒndju ˌɒslə ˈweɪbə|, |ˈrɛndju ˌɒslə ˈweɪbə|, U.S. |ˈrɑndju ˌɑslər ˈwɛbər|
[‹ the names of Henri J. L. M. Rendu, William Osler, and Frederick P. Weber (see Osler–Weber–Rendu n.). Compare slightly later Osler–Rendu–Weber n., Osler–Weber–Rendu n.
Compare the following isolated earlier attestation of Rendu-Weber-Osler:
1940S. Afr. Med. Jrnl. 14 305/1 (heading) A case of hereditary multiple telangiectasia (Rendu-Weber-Osler disease). ]
Rendu–Osler–Weber disease n. = hereditary haemorrhagic telangiectasia n. at hereditary adj. and n. Additions. Cf. Osler–Weber–Rendu n. Also Rendu–Osler–Weber's disease, Rendu–Osler–Weber syndrome.
1957Bull. Los Angeles Neurol. Soc. 22 28 (title) Encephalic lesions in hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber disease); report of case with the disclosure of microscopic telangiectasis in the leptomeninges. 1984Amer. Jrnl. Genetics 19 19 Interest in Rendu-Osler-Weber (ROW) syndrome has been renewed because of new treatment for the pulmonary artery fistulae that occur in approximately one-half of the patients. 2001Jrnl. Ultrasound in Med. 106214 Hereditary hemorrhagic telangiectasia or Rendu-Osler-Weber disease provides an example of the genetic disorder of angiogenesis in which a multisystemic angiodysplasia is responsible for severe hemorrhage. |