| DMD | Duchenne type Muscular Dystrophy; 악성형 Duchenne형 근이영양증 |
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| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| DD | dangerous drug; data definition; day of delivery; degenerated disc; degenerative disease; delusional... |
| DMD | disease-modifying drug; Doctor of Dental Medicine; Duchenne muscular dystrophy; dystonia musculorum ... |
| DMD | Duchenne type muscular dystrophy |
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| Aran-Duchenne disease | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
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| Duchenne | Guillaume B.A., French neurologist, 1806-1875. See: Duchenne's disease, Duchenne's sign, Duchenne's syndrome, Duchenne-Aran disease, Aran-Duchenne disease, Duchenne-Erb paralysis, Duchenne dystrophy. (05 Mar 2000) |
| Duchenne-Aran disease | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| Duchenne dystrophy | The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females). Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy. (05 Mar 2000) |
| Duchenne-Erb paralysis | A type of brachial birth palsy in which there is paralysis of the muscles of the upper arm and shoulder girdle (deltoid, biceps, brachialis, and brachioradialis muscles) due to a lesion of the upper trunk of the brachial plexus or of the roots of the fifth and sixth cervical roots. Synonym: Duchenne-Erb paralysis, Erb paralysis. (05 Mar 2000) |
| Duchenne muscular dystrophy | A specific form of muscular dystrophy that is inherited as a sex-linked recessive trait and thus confined to young males and to females with Turner's syndrome. One third of all cases are estimated to be new mutational events. See: dystrophin. It is characterised by degeneration and necrosis of skeletal muscle fibres, that are replaced by fat and fibrous tissue. Symptoms include muscle weakness and in some forms, the appearance of muscle enlargement (pseudo-hypertrophy). Advanced cases can include weakness of the respiratory muscles (compromising breathing) and cardiomyopathy. Inheritance: sex-linked recessive. Incidence: 1 in 4000 male births. (11 Nov 1997) |
| Duchenne's disease | The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females). Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy. (05 Mar 2000) |
| Duchenne's sign | <clinical sign> Falling in of the epigastrium during inspiration in paralysis of the diaphragm. (05 Mar 2000) |
| Duchenne's syndrome | <syndrome> Subacute or chronic anterior spinal paralysis combined with multiple neuritis. (05 Mar 2000) |
| Duchenne's d. |
1. spinal muscular atrophy. 2. bulbar paralysis. 3. tabes dorsalis. 4. Duchenne's muscular dystrophy.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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