| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
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| MDPK | myotonic dystrophy protein kinase |
| MMD | mass median diameter; minimum morbidostatic dose; moyamoya disease; myotonic muscular dystrophy |
| MyD | myotonic dystrophy |
| MyMD | myotonic muscular dystrophy |
| CMD | Congenital myotonic dystrophy |
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| MD | Myotonic Dystrophy |
| MyD | Myotonic Dystrophy |
| MMD | Myotonic muscular dystrophy |
| MyD | Myotonic muscular dystrophy |
| myotonic | Pertaining to or exhibiting myotonia. (05 Mar 2000) |
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| myotonic cataract | Cataract occurring in myotonic dystrophy. (05 Mar 2000) |
| myotonic dystrophy | <neurology> An inherited human neuromuscular disease classed as an autosomal dominant disease in which there is progressive muscle weakening and wasting. A triplet repeat syndromes (like fragile X syndrome), this most common adult form of muscular dystrophy is caused by expansion of the unstable trinucleotide repeat CTG in the 3' untranslated region on chromosome 19q13 (cAMP-dependent muscle protein kinase gene). Anticipation has been associated with further expansion of the repeat upon transmission to subsequent generations (the inheritance pattern is autosomal dominant), although contraction has been noted to occur as well. Especially severe neonatal cases have been born to affected mothers preferentially, suggesting a role for genomic imprinting as well. The classic physical signs include atrophy of facial muscles, cataracts, and delayed muscle relaxation. Detection of the expanded trinucleotide repeat is accomplished by PCR or Southern blot and expansion appears to correlate with decreased transcription of the protein kinase gene. Inheritance: autosomal dominant. (29 Dec 1997) |
| dystrophy, myotonic | Inherited disease with myotonia (irritability and prolonged contraction of muscles), mask-like face, premature balding, cataracts, and cardiac disease. Due to a trinucleotide repeat (a stuttering sequence of three bases) in the DNA. (12 Dec 1998) |
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Synonyms : Eulenburg Disease, Eulenburg's Disease, PROMM (Proximal Myotonic Myopathy), Proximal Myotonic Myopathy, Congenita, Paramyotonia, Disease, Eulenburg, Disease, Eulenburg's, Disorder, Myotonic, Disorders, Myotonic, Eulenburgs Disease, Fluctuans, Myotonia
Synonyms : Congenital Myotonic Dystrophy, Myotonia Atrophica, Myotonia Dystrophica, Steinert's Disease, Congenital Myotonic Dystrophies, Dystrophies, Congenital Myotonic, Dystrophies, Myotonic, Dystrophy, Congenital Myotonic, Dystrophy, Myotonic, Myotonic Dystrophies
| myotonic |
of or relating to or caused by myotonia
출처: wordnet.princeton.edu/perl/webwn
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| myotonic dystrophy |
myotonic muscular dystrophy: a severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant
출처: wordnet.princeton.edu/perl/webwn
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| myotonic dystrophy |
Myotonic dystrophy (DM) is a chronic, slowly progressing, highly variable inherited disease that can manifest at any age from birth to old age. It is characterized by a wasting of the muscles (muscular dystrophy), opacity of the lens of the eyes (cataracts), heart conduction defects and myotonia (difficulty relaxing a muscle). ...
출처: en.wikipedia.org/wiki/Myotonic_dystrophy
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| myotonic discharge |
high frequency repetitive discharges seen in myotonia and evoked by insertion of a needle electrode, percussion of a muscle, or stimulation of a muscle or its motor nerve; characterized by waxing and waning of frequency and amplitude. There are two types: one with biphasic spike potentials resembling fibrillation potentials and one with waves resembling positive sharp waves.
출처: www.merckmedicus.com/pp/us/hcp/thcp_dorlands_conte...
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| myotonic dystrophy |
a rare, slowly progressive, hereditary disease transmitted as an autosomal dominant trait, characterized by myotonia followed by atrophy of the muscles (especially those of the face and neck), cataracts, hypogonadism, frontal balding, and cardiac abnormalities; called also dystrophia myotonica, myotonia atrophica, and Steinert's disease.
출처: www.merckmedicus.com/pp/us/hcp/thcp_dorlands_conte...
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| myotonic | of or relating to or caused by myotonia |
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| myotonic | a severe form of muscular dystrophy marked by facial weakness and drooping eyelids and difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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