Wilson disease

Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.

Cholestasis

Impairment of bile flow due to obstruction in bile ducts.


Total: 4

                       


(per page)
PMID (PMCID)
31145285
 MALE
Persistent cholestasis resulting from duodenal papillary carcinoma in an adolescent male: A case report.
Fu H, Li Y, Bai G, Yin R, Yin C, Shi W, Zhang L, Li R, Zhao R.
Medicine (Baltimore). 2019;98(22):e15708.
Additional laboratory tests eliminated common causes of cholestasis such as bacterial/viral infection, autoimmune liver disease, Wilson disease, Alagille syndrome, or progressive familial intrahepatic cholestasis type 3.
22720273
 MALE
Alagille syndrome and Wilson disease in siblings: a diagnostic conundrum.
Amson M, Lamoureux E, Hilzenrat N, Tischkowitz M.
Can J Gastroenterol. 2012;26(6):330-2.
The index case, the 18-year-old asymptomatic brother of a young man recently diagnosed with Wilson disease, presented for Wilson disease screening and was also found to have abnormal liver function suggestive of cholestasis.
22720273
 MALE
Alagille syndrome and Wilson disease in siblings: a diagnostic conundrum.
Amson M, Lamoureux E, Hilzenrat N, Tischkowitz M.
Can J Gastroenterol. 2012;26(6):330-2.
The index case, the 18-year-old asymptomatic brother of a young man recently diagnosed with Wilson disease, presented for Wilson disease screening and was also found to have abnormal liver function suggestive of cholestasis.
20422502
 FEMALE Young Adult
A patient with persistent pruritus.
Liu LU, Qin L, Knisely AS.
Semin Liver Dis. 2010;30(2):205-9.
Laboratory and radiology test results eliminated the possibility of acute hepatitis A/B/C viral infections, primary biliary cirrhosis, autoimmune hepatitis, Wilson disease, paraneoplastic cholestasis, and obstructive biliary disease.