Wilson's disease [(WD), or hepatolenticular degeneration, is an autosomal recessive disorder with a prevalence of 1:50,000 to 1:100,000 live births.[1] The metabolism disturbance of copper for lack of ceruloplasmin leads to neuropsychiatric and hepatic symptoms such as tremor, seizures, chronic hepatitis, and even acute liver failure.[2] The excessive copper accumulation in the uterus of women results in poor pregnancy rate and recurrent miscarriage of women with WD.[1] Zinc sulphate as an effective therapy could be helpful for successful pregnancy outcomes. Here, CP is linked to Wilson disease.