| Literature DB >> 17236903 |
T Andrew Burrow1, Mitchell B Cohen, Ronald Bokulic, Gail Deutsch, Arabinda Choudhary, Richard A Falcone, Gregory A Grabowski.
Abstract
A 5-year-old male with Gaucher's disease type 3 developed progressive mesenteric and mediastinal lymphadenopathy over 12 months, despite enzyme replacement therapy, contributing to the development of a protein-losing enteropathy. These complications are unique, indicating poorly accessible, differentially responsive compartments in patients with Gaucher's disease who are receiving enzyme therapy.Entities:
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Year: 2007 PMID： 17236903 DOI： 10.1016/j.jpeds.2006.10.062
Source DB: PubMed Journal: J Pediatr ISSN： 0022-3476 Impact factor: 4.406