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Early HSCT corrects the skeleton in MPS.

Authors :
Kurtzberg J
Source :
Blood [Blood] 2015 Mar 05; Vol. 125 (10), pp. 1518-9.
Publication Year :
2015

Abstract

In this issue of Blood, Pievani et al have identified a potential solution to the remaining barrier to the success of hematopoietic stem cell transplantation (HSCT) in children with severe phenotype Hurler syndrome (mucopolysaccharidosis type I [MPS I]).

Details

Language :
English
ISSN :
1528-0020
Volume :
125
Issue :
10
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
25745184
Full Text :
https://doi.org/10.1182/blood-2014-11-606681