Add to ORKGWilson\u27s disease (WD) is a rare autosomal recessive disorder of copper metabolism. Data regarding WD is not available from Pakistan. A cross-sectional study was conducted at The Aga Khan University Hospital, Karachi, and all patients admitted with primary and secondary diagnosis of Wilson\u27s disease were added. A total of 47 patients were seen; 68% (n = 32) were male. The mean age was 26.6 ± 9.97 years. Most of the patients presented with hepatic, (n = 22, 46.8%), neurological, (n = 17, 36.2%) and psychiatric (n = 8, 17%) symptoms. Mean ceruloplasmin level was 0.17 ± 0.13 g/dl; it was \u3c 0.25 g/dl in 39 (86.6%) patients. Serum copper (Cu) was reduced in 32 (68.1%) patients and 24-hr-urinary Cu was raised in 22 (47.6%) patients. Sli...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Background: Wilson’s disease is an autosomal recessive disorder due to mutation in ATB 7B gene, whi...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...
Wilson\u27s disease (WD) is a rare autosomal recessive disorder of copper metabolism. Data regarding...
Wilson′s disease (WD) is an autosomal recessive disease involving a defect of copper transport by th...
Wilson′s disease (WD) is an autosomal recessive disease involving a defect of copper transport by th...
Wilson disease (WND) is an autosomal recessive disorder caused by mutation in ATP7B gene that impair...
Wilson's disease is an autosomal recessive disorder of copper metabolism. The culprit gene is ATP7B....
Wilson’s disease (WD) is a rare autosomal recessive disorder of hepatocellular copper deposition. Th...
WOS: 000360663100023Wilson disease (WD) is an autosomal recessive disorder of copper transport cause...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson's disease (WD) is an autosomal recessive disorder, resulting from variations in ATP7B gene. C...
Wilson’s disease is a rare, inherited autosomal recessive disease of copper metabolism, in which the...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Background: Wilson’s disease is an autosomal recessive disorder due to mutation in ATB 7B gene, whi...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...
Wilson\u27s disease (WD) is a rare autosomal recessive disorder of copper metabolism. Data regarding...
Wilson′s disease (WD) is an autosomal recessive disease involving a defect of copper transport by th...
Wilson′s disease (WD) is an autosomal recessive disease involving a defect of copper transport by th...
Wilson disease (WND) is an autosomal recessive disorder caused by mutation in ATP7B gene that impair...
Wilson's disease is an autosomal recessive disorder of copper metabolism. The culprit gene is ATP7B....
Wilson’s disease (WD) is a rare autosomal recessive disorder of hepatocellular copper deposition. Th...
WOS: 000360663100023Wilson disease (WD) is an autosomal recessive disorder of copper transport cause...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson's disease (WD) is a copper metabolism disorder that is inherited in an autosomal recessive ma...
Wilson's disease (WD) is an autosomal recessive disorder, resulting from variations in ATP7B gene. C...
Wilson’s disease is a rare, inherited autosomal recessive disease of copper metabolism, in which the...
Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the liver and s...
Wilson disease is an autosomal recessive copper storage disease. It is characterized by an inability...
Background: Wilson’s disease is an autosomal recessive disorder due to mutation in ATB 7B gene, whi...
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to ...