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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2021
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| Materias: | |
| 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 |