| Literature DB >> 18819128 |
Ami J Shah1, Neena Kapoor, Robert M Cooper, Gay M Crooks, Carl Lenarsky, Hisham Abdel-Azim, Shi Qi Wu, Kathy Wilson, Kenneth I Weinberg, Robertson Parkman, Donald B Kohn.
Abstract
Hemophagocytic lymphohistiocytosis (HLH) is a rare autosomal recessive disorder of infancy and childhood that is invariably fatal if not treated. We report on the first patient to receive post-natal HSCT for HLH after receiving in utero chemotherapy for disease stabilization.Entities:
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Year: 2009 PMID: 18819128 PMCID: PMC2592085 DOI: 10.1002/pbc.21778
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167