학술논문
Successful allogeneic cord blood transplantation in a patient with Evans syndrome leads to correction of hereditary angioedema type I as secondary effect.
Document Type
Article
Author
Source
Subject
*LETTERS to the editor
*ANGIONEUROTIC edema
*STEM cell transplantation
*THERAPEUTICS
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Language
ISSN
0268-3369
Abstract
A letter to the editor is presented which discusses the medical case of a seven-year-old boy with Evans syndrome (ES) and hereditary angioedema which were cured by an allogenic cord blood stem cells transplantation (SCT).