单词 | meige disease |
释义 | > as lemmasMeige disease 1. attributive and in the genitive. Designating a familial (autosomal dominant) form of lymphoedema, typically developing around the time of puberty and affecting the legs. Esp. in Meige disease. Cf. Milroy's disease n. ΘΚΠ the world > health and disease > ill health > a disease > congenital or hereditary syndromes > [adjective] Meige1950 nemaline1963 Down1964 1950 Acta Medica Scandinavica 137 198 (title) Chronic hereditary lymphedema (Nonne–Milroy–Meige's disease).] 1950 Acta Medica Scandinavica 137 208 Chronic hereditary edema is usually divided into 2 groups: (1) congenital edema of the Nonne–Milroy type, and (2) late or tardive edema of the Meige type. 1962 Amer. Jrnl. Med. 32 651/1 It is the purpose of this paper to report a case of familial lymphedema of the Meige's type. 1962 H. O. Mackey Handbk. Dis. Skin (ed. 7) xxviii. 307 Hereditary oedema of the legs. (Milroy's disease; Meige's disease). 1983 Cleft Palate Jrnl. 20 151 Meige disease (familial lymphedema praecox) and cleft palate: report of a family and review of the literature. 1998 European Jrnl. Dermatol. 8 511 Lymphangiosarcoma can exceptionally arise in congenital hereditary lymphedema (Milroy's syndrome and Meige's syndrome). < as lemmas |
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