Nada Muidh Aloufi

Epidemiology, Evaluation and Management of Wilson Disease: Review Article

Mohammed Salah Hussein, Turki Mohammed A. Alshehri, Nada Muidh Aloufi, Alghamdi, Ibrahim Saeed A., Al zahrani, Adel Abdulrahman S., Fahad Ayed Alharbi, Ahmed Abdulaziz A. Alqerafi, Alsarraj, Nawaf Faiq M, Manal Abdulrahman Alem & Alotaibi. Saad Jamal · Journal of Pharmaceutical Research International · 2021

Wilson disease (hepatolenticular degeneration) is a rare autosomal recessive ailment characterized by aberrant copper buildup in the body, with the brain, liver, and cornea being notably affected. Wilson illness is caused by a mutation in the ATP7B gene on chromosome 13, which re...