Complications of Evans' syndrome in an infant with hereditary spherocytosis: a case report

Hereditary spherocytosis (HS) is a genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice and splenomegaly. Evans' syndrome is a clinical syndrome characterized by autoimmune hemolytic anemia (AIHA) accompanied by immune thrombocytopenic purpura (ITP). It r...

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Bibliographic Details
Main Authors: Yoshida, Hideki, Ishida, Hiroyuki, Yoshihara, Takao, Oyamada, Takashi, Kuwana, Masataka, Imamura, Toshihiko, Morimoto, Akira
Format: Artigo
Language:Inglês
Published: BioMed Central 2009
Subjects:
Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2753340/
https://ncbi.nlm.nih.gov/pubmed/19740448
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-8722-2-40
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