Meigen.

Brit.

/ˈmʌɪɡə/,

/meɪdʒ/, U.S.

/ˈmaɪɡə/,

/meɪdʒ/

Origin: From a proper name. Etymon: proper name Meige.

Etymology: < the name of Henri Meige, French neurologist (1866–1940), who described the two disorders (1898, in Presse médicale 6 341 and 1910, in Rev. neurol. Paris 2 437 respectively).

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).

2. attributive and in the genitive. Designating a neurological disorder characterized by blepharospasm and oromandibular dystonia (spasmodic contraction of the muscles of the eyelids, mouth, tongue, and jaw), typically beginning in or beyond middle age. Esp. in Meige's syndrome.

ΘΚΠ

the world > health and disease > ill health > a disease > disorders of internal organs > disorders of nervous system > [adjective] > other nervous disorders

Tourette1899

ciguatoxic1965

Meige1972

the world > health and disease > ill health > a disease > diseases of tissue > disorders affecting muscles > [adjective] > spasm or cramp > qualities or types

synclonic1822

ergotic1875

saltatoric spasm1877

saltatory1881

neuroclonic1899

dystonic1917

Meige1972

1972 Geriatrics 27 69 One of the many movement disorders involving the face is Meige's syndrome, so termed in this report in recognition of Meige's early description.

1986 Jrnl. Otolaryngol. 15 306 Essential blepharospasm is considered to be an incomplete form of Meige dystonic syndrome.

1990 Functional Neurol. 5 165 Meige's disease is a form of focal dystonia characterized by symmetric dystonic spasms of facial muscles, sometimes associated with dystonic movements of other midline muscle groups.

2001 Omaha (Nebraska) World-Herald (Nexis) 23 Apr. 27 Meige's syndrome affects not only the eyelids but also cheek and neck muscles.

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

单词	meige
释义	Meigen. Brit. /ˈmʌɪɡə/, /meɪdʒ/, U.S. /ˈmaɪɡə/, /meɪdʒ/ Origin: From a proper name. Etymon: proper name Meige. Etymology: < the name of Henri Meige, French neurologist (1866–1940), who described the two disorders (1898, in Presse médicale 6 341 and 1910, in Rev. neurol. Paris 2 437 respectively). 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). 2. attributive and in the genitive. Designating a neurological disorder characterized by blepharospasm and oromandibular dystonia (spasmodic contraction of the muscles of the eyelids, mouth, tongue, and jaw), typically beginning in or beyond middle age. Esp. in Meige's syndrome. ΘΚΠ the world > health and disease > ill health > a disease > disorders of internal organs > disorders of nervous system > [adjective] > other nervous disorders Tourette1899 ciguatoxic1965 Meige1972 the world > health and disease > ill health > a disease > diseases of tissue > disorders affecting muscles > [adjective] > spasm or cramp > qualities or types synclonic1822 ergotic1875 saltatoric spasm1877 saltatory1881 neuroclonic1899 dystonic1917 Meige1972 1972 Geriatrics 27 69 One of the many movement disorders involving the face is Meige's syndrome, so termed in this report in recognition of Meige's early description. 1986 Jrnl. Otolaryngol. 15 306 Essential blepharospasm is considered to be an incomplete form of Meige dystonic syndrome. 1990 Functional Neurol. 5 165 Meige's disease is a form of focal dystonia characterized by symmetric dystonic spasms of facial muscles, sometimes associated with dystonic movements of other midline muscle groups. 2001 Omaha (Nebraska) World-Herald (Nexis) 23 Apr. 27 Meige's syndrome affects not only the eyelids but also cheek and neck muscles. This is a new entry (OED Third Edition, March 2004; most recently modified version published online March 2022). < n.1950
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