| Dubin-Johnson syndrome |
An inherited form of the jaundice. This is a metabolic abnormality that is benign.
Ãâó: 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.
Ãâó: 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.
Ãâó: 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.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Dubin-Sprinz syndrome |
Dubin-Johnson syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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