Immunoglobulin a nephropathy as the first clinical presentation of Wilson disease: a case report and literature review

BACKGROUND: Wilson disease (WD) is a rare genetic disorder of copper metabolism. Differences in copper tissue accumulation lead to various clinical manifestations, including some atypical presentations. The complex clinical features of WD make diagnosis challenging, delaying the best chance for trea...

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Detalles Bibliográficos
Autores principales: Zhang, Yong-Zhe, Jian, Geng, He, Ping, Yu, Rui, Tian, Mi, Wu, Yan, Zhang, Bei-Ru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524855/
https://www.ncbi.nlm.nih.gov/pubmed/34666712
http://dx.doi.org/10.1186/s12876-021-01954-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524855/
https://www.ncbi.nlm.nih.gov/pubmed/34666712
http://dx.doi.org/10.1186/s12876-021-01954-8

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