| PMD | Pelizaeus-Merzbacher disease; posterior mandibular depth; primary myocardial disease; private medici... |
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| PMD | Pelizaeus Merzbacher Disease |
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| Merzbacher | Ludwig, German physician in Argentina, 1875-1942. See: Merzbacher-Pelizaeus disease, Pelizaeus-Merzbacher disease. (05 Mar 2000) |
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| Merzbacher-Pelizaeus disease | A sudanophilic leukodystrophy with a tigroid appearance of the myelin resulting from patchy demyelination. Type 1-classic, nystagmus and tremor appearing in the first few months of life, followed by slow motor development sometimes with choreoathetosis, spasticity, optic atrophy and seizures, with death in early adulthood, X-linked recessive inheritance; type 2-contralateral form with death in months to years after birth, X-linked recessive inheritance; type 3-transitional, with death in the first decade; type 4-adult form associated with involuntary movements, ataxia and hyperreflexia, but without nystagmus; type 5-variant forms. Cockayne is sometimes included as a sixth form. Synonym: Merzbacher-Pelizaeus disease. (05 Mar 2000) |
| Pelizaeus-Merzbacher disease | A sudanophilic leukodystrophy with a tigroid appearance of the myelin resulting from patchy demyelination. Type 1-classic, nystagmus and tremor appearing in the first few months of life, followed by slow motor development sometimes with choreoathetosis, spasticity, optic atrophy and seizures, with death in early adulthood, X-linked recessive inheritance; type 2-contralateral form with death in months to years after birth, X-linked recessive inheritance; type 3-transitional, with death in the first decade; type 4-adult form associated with involuntary movements, ataxia and hyperreflexia, but without nystagmus; type 5-variant forms. Cockayne is sometimes included as a sixth form. Synonym: Merzbacher-Pelizaeus disease. (05 Mar 2000) |
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| pelizaeus-merzbacher syndrome | <radiology> Slowly progressive dysmyelinating disease, diffuse, symmetrical demyelination, cerebrum, cerebellum, brainstem, spinal cord, islands of partially demyelinated fibres, CT may be normal, two types: X-linked recessive (presents in infancy), autosomal dominant (preadulthood) (12 Dec 1998) |
| Merzbacher-Pelizaeus d. |
Pelizaeus-Merzbacher d.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Merzbacher-Pelizaeus disease |
Pelizaeus-Merzbacher disease; see under disease.
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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