Osler–Rendu–Webern.

Brit.

/ˌɒsləˌrɒndjuːˈwɛbə/,

/ˌɒsləˌrɒndjuːˈveɪbə/, U.S.

/ˌɑslərˌrɑnd(j)uˈwɛbər/

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

Etymology: < the names of William Osler (see Osler n.), Henri J. L. M. Rendu, and Frederick P. Weber (see Rendu–Osler–Weber n.). Compare earlier Rendu–Osler–Weber n., and Osler–Weber–Rendu n.

Medicine.

= Rendu–Osler–Weber n.

ΚΠ

1954 Acta Pathol. & Microbiol. Scand. 35 332 (title) On the pathogenesis of hepatic changes in telangiectasia hereditaria haemorrhagica (morbus Osler-Rendu-Weber).]

1957 Amer. Jrnl. Med. 22 680/1 One might mention multiple exostoses, tuberose sclerosis, Osler-Rendu-Weber telangiectasia, Ollier's enchondromatosis, [etc.].

1961 Ohio Med. 57 899 (title) Osler-Rendu-Weber disease. Report of a case with repeated gastrointestinal hemorrhage.

1987 D. J. Weatherall et al. Oxf. Textbk. Med. (ed. 2) II. xix. 225/1 Hereditary haemorrhagic telangiectasia (Osler–Rendu–Weber syndrome). This dominantly inherited condition usually becomes clinically manifest at puberty or later.

2005 Arch. Med. Res. 36 472/2 First positive experiences could be gained in the treatment of patients with hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Rendu-Weber's disease.

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

单词	osler–rendu–weber
释义	Osler–Rendu–Webern. Brit. /ˌɒsləˌrɒndjuːˈwɛbə/, /ˌɒsləˌrɒndjuːˈveɪbə/, U.S. /ˌɑslərˌrɑnd(j)uˈwɛbər/ Origin: From proper names. Etymons: proper names Osler, Rendu, Weber. Etymology: < the names of William Osler (see Osler n.), Henri J. L. M. Rendu, and Frederick P. Weber (see Rendu–Osler–Weber n.). Compare earlier Rendu–Osler–Weber n., and Osler–Weber–Rendu n. Medicine. = Rendu–Osler–Weber n. ΚΠ 1954 Acta Pathol. & Microbiol. Scand. 35 332 (title) On the pathogenesis of hepatic changes in telangiectasia hereditaria haemorrhagica (morbus Osler-Rendu-Weber).] 1957 Amer. Jrnl. Med. 22 680/1 One might mention multiple exostoses, tuberose sclerosis, Osler-Rendu-Weber telangiectasia, Ollier's enchondromatosis, [etc.]. 1961 Ohio Med. 57 899 (title) Osler-Rendu-Weber disease. Report of a case with repeated gastrointestinal hemorrhage. 1987 D. J. Weatherall et al. Oxf. Textbk. Med. (ed. 2) II. xix. 225/1 Hereditary haemorrhagic telangiectasia (Osler–Rendu–Weber syndrome). This dominantly inherited condition usually becomes clinically manifest at puberty or later. 2005 Arch. Med. Res. 36 472/2 First positive experiences could be gained in the treatment of patients with hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Rendu-Weber's disease. This is a new entry (OED Third Edition, September 2004; most recently modified version published online March 2022). < n.1957
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