Homozygous α-Thalassemia Treated with Intrauterine Transfusions and Unrelated Donor Hematopoietic Cell Transplantation

Joanna S. Yi, Christopher L. Moertel, K. Scott Baker

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

Recently, intrauterine transfusions and hematopoietic cell transplantation (HCT) have changed homozygous alpha-thalassemia from a frequently fatal disease to a potentially survivable condition. We present a patient with Hemoglobin Bart's disease who was cured after failing to engraft with 1 unrelated HCT, but engrafting after a second unrelated donor HCT.

Original languageEnglish (US)
Pages (from-to)766-768
Number of pages3
JournalJournal of Pediatrics
Volume154
Issue number5
DOIs
StatePublished - May 2009

Bibliographical note

Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.

Fingerprint

Dive into the research topics of 'Homozygous α-Thalassemia Treated with Intrauterine Transfusions and Unrelated Donor Hematopoietic Cell Transplantation'. Together they form a unique fingerprint.

Cite this