Demographics and Outcomes Related to Wilson’s Disease Patients: A Nationwide Inpatient Cohort Study

Background and objective Wilson’s disease (WD) is a rare autosomal recessive disease caused by mutations in the ATP7B gene, leading to impairment in copper excretion and subsequent accumulation primarily in the liver and brain. There is scarce data in the literature on the outcomes and cost burden o...

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Detalles Bibliográficos
Autores principales: Patel, Ankoor H, Ghattu, Meghana, Mazzaferro, Natale, Chen, Alexander, Catalano, Kaitlyn, Minacapelli, Carlos D, Rustgi, Vinod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Gastroenterology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552679/
https://www.ncbi.nlm.nih.gov/pubmed/37809179
http://dx.doi.org/10.7759/cureus.44714

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552679/
https://www.ncbi.nlm.nih.gov/pubmed/37809179
http://dx.doi.org/10.7759/cureus.44714

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