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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Detalles Bibliográficos
Autores principales: Yoshida, Hideki, Ishida, Hiroyuki, Yoshihara, Takao, Oyamada, Takashi, Kuwana, Masataka, Imamura, Toshihiko, Morimoto, Akira
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2753340/
https://www.ncbi.nlm.nih.gov/pubmed/19740448
http://dx.doi.org/10.1186/1756-8722-2-40

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2753340/
https://www.ncbi.nlm.nih.gov/pubmed/19740448
http://dx.doi.org/10.1186/1756-8722-2-40

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