| Literature DB >> 15520787 |
Laurie A Myers1, Michael S Hershfield, Wirt T Neale, Maria Escolar, Joanne Kurtzberg.
Abstract
Purine nucleoside phosphorylase deficiency is a primary immunodeficiency syndrome characterized by the triad of recurrent infection, neurologic dysfunction, and autoimmunity. This patient presented atypically with few infections and normal T-cell function. Progressive lymphopenia, ataxia, and developmental delay led to diagnosis. Umbilical cord blood transplantation corrected the immunodeficiency.Entities:
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Year: 2004 PMID: 15520787 DOI: 10.1016/j.jpeds.2004.06.075
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406