单词 | williams syndrome |
释义 | > as lemmasWilliams syndrome As a modifier, esp. in Williams syndrome, Williams elfin facies syndrome. Designating a congenital condition characterized by distinctive facial characteristics, some degree of intellectual disability, vascular abnormalities, esp. narrowing of the aorta above the aortic valve, and often hypercalcaemia.Williams syndrome results from deletion of a small part of one copy of chromosome 7, including the elastin gene. ΚΠ 1967 L. Turano et al. Progress Radiol. Internat. Congr. Series No. 105 I. 153 Two of the 4 cases in the series with supravalvular aortic stenosis had multiple peripheral stenotic lesions of the pulmonary arteries, one with a complete Williams syndrome. 1975 Jrnl. Pediatrics 86 718/1 The purpose of the present report is to present a balanced evaluation of 19 patients with the Williams elfin facies Syndrome (Williams syndrome). 1997 Independent on Sunday 11 May (Review Suppl.) 48/1 In addition to language skills, Williams syndrome children are sociable, with great awareness of body language and emotions. 2019 Sentinel (Stoke-on-Trent) (Nexis) 24 Sept. 18 Deborah discovered the rare condition of Williams syndrome, which matched a lot of Martha's traits and was later confirmed by a geneticist. < as lemmas |
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