| galactosialidosis |
an autosomal recessive disorder clinically almost indistinguishable from sialidosis, type II (q.v.), but due to deficiency of both sialidase and β-galactosidase. As in sialidosis, multiple variants occur, of increasing severity with decreasing age of onset; congenital, infantile, and juvenile forms have been identified. The defect appears to be in a protein necessary for activation or protection of the two enzymes.
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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