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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...
Autores principales: | Tateno, Yuki, Suzuki, Ryoji, Kitamura, Yukihiro |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
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 |
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