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Correction of purine nucleoside phosphorylase deficiency by transplantation of allogeneic bone marrow from a sibling.
Broome, C B; Graham, M L; Saulsbury, F T; Hershfield, M S; Buckley, R H.
Affiliation
  • Broome CB; Department of Pediatrics, Duke University Medical Center, Durham, North Carolina 27710, USA.
J Pediatr ; 128(3): 373-6, 1996 Mar.
Article in En | MEDLINE | ID: mdl-8774508
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)
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Collection: 01-internacional Database: MEDLINE Main subject: Bone Marrow Transplantation / Purine-Nucleoside Phosphorylase / Immunologic Deficiency Syndromes Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: J Pediatr Year: 1996 Document type: Article Affiliation country: United States Country of publication: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Bone Marrow Transplantation / Purine-Nucleoside Phosphorylase / Immunologic Deficiency Syndromes Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: J Pediatr Year: 1996 Document type: Article Affiliation country: United States Country of publication: United States