Dubin-Johnson syndrome is an autosomal recessive disorder which causes an increase of conjugated bilirubin without elevation of liver enzymes (ALT ...
Any condition in which the release of bile from the liver is blocked. The blockage can occur in the liver (intrahepatic cholestasis) or in the bile ducts (extrahepatic cholestasis).
Dubin-Johnson syndrome as related to Cholestasis
- Dubin–Johnson syndrome - Wikipedia, the free encyclopedia
Dubin–Johnson syndrome is an autosomal recessive disorder that causes an increase of conjugated bilirubin in the serum without elevation of liver enzymes (ALT, AST).
- Dubin-Johnson Syndrome - Medscape Reference
Dubin-Johnson syndrome is an inherited, relapsing, benign disorder of bilirubin metabolism. This rare autosomal recessive condition is characterized by ...
- Pediatric Dubin-Johnson Syndrome - Medscape Reference
Pediatric Dubin-Johnson Syndrome. First described in 1954, Dubin-Johnson syndrome (DJS) is an inherited, relapsing, benign disorder of bilirubin …
- Dubin-Johnson Syndrome | Doctor | Patient.co.uk
Synonyms: hyperbilirubinaemia II, DJS, Sprinz-Nelson syndrome This is a rare inherited disorder of bilirubin metabolism that was described by Dubin and...
- Syndrome de Dubin-Johnson - Wikipédia
208085 - arthrogryposis, renal dysfunction, and cholestasis 1; arcs1 - arc syndrome; arcs
- Jaundice: Approach to the Patient With Liver Disease ...
Jaundice in Adults: A Merck Manual of Patient Symptoms podcast. Jaundice is a yellowish discoloration of the skin and mucous membranes caused by …
- Genes Associated with Diseases - Full list - GeneCards
19,231 "disease genes" are currently present in the GeneCards database This is a partial list of 5,000 genes. The complete list contains 19,231 genes.
- Laboratory Diagnosis of Liver Disease - UCSD Lab Medicine
Disease Tests; Acute hepatitis: AST, ALT, GGT, LDH, serum bilirubin conjugated & total, viral antigens: Chronic hepatitis: ALT, AST, viral antigens, viral antibodies ...
- Stargardt disease - Wikipedia, the free encyclopedia
Stargardt disease, or fundus flavimaculatus, is an inherited form of juvenile macular degeneration that causes progressive vision loss usually to the point of legal ...