| MCR | Medical Corps Reserve; melanocortin receptor; message competition ratio; metabolic clearance rate; m... |
|---|
| myotonia atrophica | A rare, slowly progressive, hereditary disease transmitted as an autosomal dominant trait and characterised by myotonia followed by atrophy of the muscles, cataracts, hypogonadism, balding, and cardiac abnormalities. (12 Dec 1998) |
|---|
| macula atrophica | An atrophic glistening white spot on the skin. (05 Mar 2000) |
|---|---|
| hyperkeratosis figurata centrifuga atrophica | A rare, chronic, progressive autosomal dominant disorder seen most often in males and usually appearing in early childhood. It is characterised by the formation of slightly atrophic patches surrounded by an elevated, keratotic border. (12 Dec 1998) |
| myotonia | Increased muscular irritability and contractility with decreased power of relaxation; toxic spasm of muscle. (12 Dec 1998) |
| myotonia acquisita | Acquired myotonia following exposure to certain toxins. (05 Mar 2000) |
| myotonia congenita | A congenital genetic disease characterised by tonic spasm and rigidity of certain muscles when an attempt is made to move them after a period of rest or when mechanically stimulated. The stiffness disappears as the muscles are moved. (12 Dec 1998) |
| myotonia dystrophica | <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) |
| myotonia neonatorum | Hypocalcaemic tetany occurring in neonates or young infants, due to transient functional hypoparathyroidism in consumption of cow's milk (high phosphorus content). Synonym: myotonia neonatorum, tetania neonatorum, tetanism. (05 Mar 2000) |
| myotonia atrophica |
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
|
|---|
| myotonia atrophica | 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 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|