Previously undiagnosed hereditary spherocytosis in a patient with jaundice and pyelonephritis: a case report

BACKGROUND: Hereditary spherocytosis is autosomal dominant inherited extravascular hemolytic disorder and is the commonest cause of inherited hemolysis in northern Europe and the United States. The classical clinical features of hereditary spherocytosis are anemia, jaundice, and splenomegaly. Howeve...

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Detalles Bibliográficos
Autores principales: Tateno, Yuki, Suzuki, Ryoji, Kitamura, Yukihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134285/
https://www.ncbi.nlm.nih.gov/pubmed/27906107
http://dx.doi.org/10.1186/s13256-016-1144-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134285/
https://www.ncbi.nlm.nih.gov/pubmed/27906107
http://dx.doi.org/10.1186/s13256-016-1144-8

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