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Gewählte Publikation:

Urban, C; Preisegger, KH; Krugluger, W; Hopmeier, P; Schwinger, W; Lackner, H; Kerbl, R; Dornbusch, HJ; Benesch, M.
Allogeneic bone marrow transplantation in a child with hemoglobinopathy olmsted.
J Pediatr Hematol Oncol. 2002; 24(5):417-419 Doi: 10.1097%2F00043426-200206000-00020 (- Case Report)
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Führende Autor*innen der Med Uni Graz
Urban Ernst-Christian
Co-Autor*innen der Med Uni Graz
Benesch Martin
Dornbusch Hans Jürgen
Kerbl Reinhold
Lackner Herwig
Preisegger Karl Heinz
Schwinger Wolfgang
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Abstract:
The authors describe the first successful bone marrow transplant for the treatment of hemoglobinopathy Olmsted in a boy who presented with severe transfusion-dependent hemolytic anemia and jaundice at age 4 months. He received bone marrow from an HLA-identical sibling with normal hemoglobin electrophoresis after conditioning with busulfan, cyclophosphamide, and antithymocyte globulin when he was 18 months old. The posttransplant course was uneventful. Two years after transplantation the patient has a normal hemoglobin level without evidence of hemolysis. DNA analysis shows 100% chimerism of donor cell origin, confirming full engraftment with normal hematopoietic cells.
Find related publications in this database (using NLM MeSH Indexing)
Antineoplastic Agents, Alkylating - therapeutic use
Bone Marrow Transplantation - therapeutic use
Busulfan - therapeutic use
Cyclophosphamide - therapeutic use
DNA Primers - chemistry
Globins - genetics
Hemoglobinopathies - genetics
Hemoglobins, Abnormal - genetics
Humans - genetics
Infant - genetics
Male - genetics
Mutation - genetics
Polymerase Chain Reaction - genetics
Transplantation Conditioning - genetics
Transplantation, Homologous - genetics

Find related publications in this database (Keywords)
Olmsted
hemoglobinopathy
children
bone marrow transplantation
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