| DJS | Dubin-Johnson syndrome |
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| DJS | Dubin Johnson Syndrome |
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| Dubin | I. Nathan, U.S. Pathologist, 1913-1980. See: Dubin-Johnson syndrome. (05 Mar 2000) |
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| Dubin-Johnson syndrome | <syndrome> An inherited disorder (autosomal recessive) that is characterised by long-standing mild jaundice. This occurs secondary to an abnormality in the transport of bilirubin from the liver to the biliary system. This leads to an accumulation of bilirubin in the liver. Avoidance of alcohol and medications which can affect the liver is important. Inheritance: autosomal recessive. (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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두비나액 - 새창
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대화제약 |
A15602391 | Ketoconazole | 일반의약품 | 삭제 |
| Dubin-Johnson syndrome |
An inherited form of the jaundice. This is a metabolic abnormality that is benign.
출처: www.gastromd.com/definitionsd.html
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| Dubin-Johnson syndrome |
Inherited form of chronic jaundice (yellow tint to the skin and eyes) that has no known cause.
출처: www.umm.edu/digest/glossa-m.htm
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| Dubin-Johnson syndrome |
An inherited disorder characterized by mild jaundice throughout life. Dubin-Johnson syndrome is inherited as an autosomal recessive disorder. The transport of bilirubin from the liver into the biliary system is abnormal and the bilirubin accumulates in the liver.
출처: www.solvo.hu/glossary.html
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| Dubin-Johnson s. |
a familial chronic form of nonhemolytic jaundice thought to be due to a defect in the excretion of conjugated bilirubin and certain other organic anions (e.g., sulfobromophthalein) by the liver. It is characterized by the presence of a brown, coarsely granular pigment in the hepatic cells, which is pathognomonic of the condition. Called also Sprinz-Dubin s. and Sprinz-Nelson s.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Dubin-Sprinz syndrome |
Dubin-Johnson syndrome.
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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