myotonic dystrophyn.

Brit.

/mʌɪə(ʊ)ˈtɒnɪk ˈdɪstrəfi/, U.S.

/ˈˌmaɪoʊˌtɑnɪk ˈdɪstrəfi/

Origin: Formed within English, by compounding. Etymons: myotonic adj., dystrophy n. at dys- prefix .

Etymology: < myotonic adj. + dystrophy n. at dys- prefix . Compare earlier dystrophia myotonica n. at dys- prefix Additions, German myotonische Dystrophie (1918 in Münchener med. Wochenschr. 18 Dec. 1630/2), French dystrophie myotonique (1928 in Revue neurologique 1 713), and later myotonia dystrophica n.

Medicine.

A relatively common form of muscular dystrophy, characterized by autosomal dominant inheritance, weakness and wasting of muscles of the face, neck, and forearms, localized myotonia, cataracts, gonadal atrophy and frontal balding (in men), and various other abnormalities.

ΘΚΠ

the world > health and disease > ill health > a disease > diseases of tissue > disorders affecting muscles > [noun] > myotonia > disease characterized by

congenital myotonia1886

myotonia congenita1887

Thomsen's disease1890

myotonia atrophica1908

dystrophia myotonica1923

myotonic dystrophy1929

myotonia dystrophica1956

1929 Arch. Ophthalmol. 1 335 Myotonic dystrophy, dystrophia myotonica or myotonia atrophica was first identified as a clinical entity in 1890.

1938 Bull. Johns Hopkins Hosp. 62 188 A clinical study of myotonic dystrophy and myotonia congenita.

1967 Arch. Neurol. (Chicago) 16 181/1 Familial myotonic dystrophy usually has its onset in adult life and shows myotonia and muscle wasting as its principle characteristics.

1992 Sci. Amer. May 34/1 Myotonic dystrophy..seems to get worse in successive generations.

2002 Endocrinology 143 3017 Myotonic dystrophy (DM) is the most common inherited adult neuromuscular disorder.

This is a new entry (OED Third Edition, June 2003; most recently modified version published online March 2022).

单词	myotonic dystrophy
释义	myotonic dystrophyn. Brit. /mʌɪə(ʊ)ˈtɒnɪk ˈdɪstrəfi/, U.S. /ˈˌmaɪoʊˌtɑnɪk ˈdɪstrəfi/ Origin: Formed within English, by compounding. Etymons: myotonic adj., dystrophy n. at dys- prefix . Etymology: < myotonic adj. + dystrophy n. at dys- prefix . Compare earlier dystrophia myotonica n. at dys- prefix Additions, German myotonische Dystrophie (1918 in Münchener med. Wochenschr. 18 Dec. 1630/2), French dystrophie myotonique (1928 in Revue neurologique 1 713), and later myotonia dystrophica n. Medicine. A relatively common form of muscular dystrophy, characterized by autosomal dominant inheritance, weakness and wasting of muscles of the face, neck, and forearms, localized myotonia, cataracts, gonadal atrophy and frontal balding (in men), and various other abnormalities. ΘΚΠ the world > health and disease > ill health > a disease > diseases of tissue > disorders affecting muscles > [noun] > myotonia > disease characterized by congenital myotonia1886 myotonia congenita1887 Thomsen's disease1890 myotonia atrophica1908 dystrophia myotonica1923 myotonic dystrophy1929 myotonia dystrophica1956 1929 Arch. Ophthalmol. 1 335 Myotonic dystrophy, dystrophia myotonica or myotonia atrophica was first identified as a clinical entity in 1890. 1938 Bull. Johns Hopkins Hosp. 62 188 A clinical study of myotonic dystrophy and myotonia congenita. 1967 Arch. Neurol. (Chicago) 16 181/1 Familial myotonic dystrophy usually has its onset in adult life and shows myotonia and muscle wasting as its principle characteristics. 1992 Sci. Amer. May 34/1 Myotonic dystrophy..seems to get worse in successive generations. 2002 Endocrinology 143 3017 Myotonic dystrophy (DM) is the most common inherited adult neuromuscular disorder. This is a new entry (OED Third Edition, June 2003; most recently modified version published online March 2022). < n.1929
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