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J Pediatr ; 128(3): 373-6, 1996 Mar.
Article in English | MEDLINE | ID: mdl-8774508

ABSTRACT

Deficiency of the purine salvage pathway enzyme purine nucleoside phosphorylase causes a combined immunodeficiency and neurologic abnormalities and is usually fatal in childhood. We report the first successful transplantation of bone marrow from a sibling with identical class II human leukocyte antigens in this condition, demonstrating correction of both lymphocyte metabolic and functional abnormalities.


Subject(s)
Bone Marrow Transplantation , Immunologic Deficiency Syndromes/etiology , Immunologic Deficiency Syndromes/therapy , Purine-Nucleoside Phosphorylase/deficiency , Child , Follow-Up Studies , Histocompatibility Testing , Humans , Purine-Pyrimidine Metabolism, Inborn Errors/complications , Purine-Pyrimidine Metabolism, Inborn Errors/enzymology , Time Factors , Transplantation, Homologous
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