Rendu–Osler–Webern.

Brit.

/ˌrɒndjuːˌɒsləˈwɛbə/,

/ˌrɒndjuːˌɒsləˈveɪbə/, U.S.

/ˌrɑnd(j)uˌɑslərˈwɛbər/

Origin: From proper names. Etymons: proper names Rendu, Osler, Weber.

Etymology: < the names of Henri J. L. M. Rendu (1844–1902), French physician,William Osler (see Osler n.), and Frederick P. Weber (1863–1962), British physician, each of whom independently described the disease. Compare later Osler–Rendu–Weber n. and Osler–Weber–Rendu n.Rendu described the condition in 1896 ( Bull. de la Soc. Méd. des Hôpitaux de Paris 13 731), Osler in 1901 ( Bull. Johns Hopkins Hosp. 12 333), and Weber in 1904 ( Edinb. Med. Jrnl. 15 346).

Medicine.

attributive and in the genitive, esp. in Rendu–Osler–Weber disease. Designating the disorder hereditary haemorrhagic telangiectasia. Cf. Osler–Rendu–Weber n., Osler–Weber–Rendu n.

ΚΠ

1931 Arch. Internal Med. 48 852 Perhaps his cases were instances of Rendu-Osler-Weber's disease, and not hemophilia.

1984 Amer. Jrnl. Med. 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.

2001 Acta Haematologica 106 214/1 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.

This is a new entry (OED Third Edition, September 2004; most recently modified version published online March 2022).

单词	rendu–osler–weber
释义	Rendu–Osler–Webern. Brit. /ˌrɒndjuːˌɒsləˈwɛbə/, /ˌrɒndjuːˌɒsləˈveɪbə/, U.S. /ˌrɑnd(j)uˌɑslərˈwɛbər/ Origin: From proper names. Etymons: proper names Rendu, Osler, Weber. Etymology: < the names of Henri J. L. M. Rendu (1844–1902), French physician,William Osler (see Osler n.), and Frederick P. Weber (1863–1962), British physician, each of whom independently described the disease. Compare later Osler–Rendu–Weber n. and Osler–Weber–Rendu n.Rendu described the condition in 1896 ( Bull. de la Soc. Méd. des Hôpitaux de Paris 13 731), Osler in 1901 ( Bull. Johns Hopkins Hosp. 12 333), and Weber in 1904 ( Edinb. Med. Jrnl. 15 346). Medicine. attributive and in the genitive, esp. in Rendu–Osler–Weber disease. Designating the disorder hereditary haemorrhagic telangiectasia. Cf. Osler–Rendu–Weber n., Osler–Weber–Rendu n. ΚΠ 1931 Arch. Internal Med. 48 852 Perhaps his cases were instances of Rendu-Osler-Weber's disease, and not hemophilia. 1984 Amer. Jrnl. Med. 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. 2001 Acta Haematologica 106 214/1 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. This is a new entry (OED Third Edition, September 2004; most recently modified version published online March 2022). < n.1931
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