Wilson’s disease: a review

HIGHLIGHTS

  • who: Amie Vidyani et al. from the Division of Gastroentero-Hepatology, Department of Internal Medicine, Faculty of Medicine, Universitas Airlangga, DrSoetomo General Academic Hospital, Surabaya, Indonesia have published the research: Wilsonu2019s Disease: A Review, in the Journal: (JOURNAL)
  • what: Wilson`s disease is genetic and causes excess copper accumulation in the liver and/or brain.

SUMMARY

    Wilson`s disease is a hereditary copper transport disorder characterized by ATP7B copper-binding protein dysfunction (Hedera, 2017). Therapeutic determinations in this disease must also be considered carefully because there are differences in treatment in . . .

     

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