| ICF(M)A | International Cystic Fibrosis (Mucoviscidosis) Association |
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| mucoviscidosis | An old name (but one that has prevailed in france and some other nations) for cystic fibrosis (cf), one of the most common and serious of all genetic (inherited) diseases. The cf gene is carried by 1/20 persons (in caucasian populations) and 1 in 400 couples is at risk for having children with cf. Cf is characterised by the production of abnormal secretions leading to mucous build-up. Which can impair the pancreas (and, secondarily, the intestine). Cf mucous build-up in lungs can impair respiration. Without treatment, cf results in death for 95% of children before age 5. Early diagnosis of cf is of great importance. Early and continuing treatment of cf is valuable. (12 Dec 1998) |
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| mucoviscidosis |
cystic fibrosis: the most common congenital disease; the child's lungs and intestines and pancreas become clogged with thick mucus; caused by defect in a single gene; there is no cure
출처: wordnet.princeton.edu/perl/webwn
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| mucoviscidosis |
Generally referred to as Cystic Fibrosis in the United States
출처: www.cystic-l.org/handbook/html/glossary.htm
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| mucoviscidosis | the most common congenital disease |
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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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