Acute liver failure with hemolytic anemia in children with Wilson’s disease: Genotype-phenotype correlations?

BACKGROUND: Wilson’s disease (WD) is a rare autosomal recessive inherited disorder of copper metabolism. Acute liver failure (ALF) and hemolytic anemia represent the most severe presentation of WD in children. No clear genotype-phenotype correlations exist in WD. Protein-truncating nonsense, frame-s...

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Detalles Bibliográficos
Autores principales: Pop, Tudor Lucian, Grama, Alina, Stefanescu, Ana Cristina, Willheim, Claudia, Ferenci, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Retrospective Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568583/
https://www.ncbi.nlm.nih.gov/pubmed/34786177
http://dx.doi.org/10.4254/wjh.v13.i10.1428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568583/
https://www.ncbi.nlm.nih.gov/pubmed/34786177
http://dx.doi.org/10.4254/wjh.v13.i10.1428

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