A Case of Wilson’s Disease Presenting with Persistant Hemolysis
Vrinda Vijayakumari, Kaliyannan Mayilananthi, Durga Krishnan, Ramprasath Anbazhagan & Gaurav Narayanan · Journal of Pharmaceutical Research International · 2021
Wilson’s disease is one the rare autosomal recessive disorders of copper metabolism due to mutation in ATP7B gene located in chromosome 13. The mutations of this gene cause accumulation of copper in different tissues such as brain, liver, and eyes. The clinical presentation usual...
Open access
Research Article
10.9734/jpri/2021/v33i55B33850