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Wilson’s Disease: Diagnosis in Novel Way

Wilson’s disease first described by Kinnier Wilson in 1912, is a rare autosomal recessive genetic disorder involving a defect in copper metabolism. This disease affects between one in 30,000 to one in 100,000 individuals and has a carrier frequency of one in every 90. It is characterized by hepatic...

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Detalles Bibliográficos
Autores principales:	Kannauje, Pankaj K, Pandit, Vinay R, Wasnik, Preetam N, Das, Pranita, Venkatesan, Nanditha
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2021
Materias:	Internal Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8583229/ https://www.ncbi.nlm.nih.gov/pubmed/34790438 http://dx.doi.org/10.7759/cureus.18650

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