Article (Published version) (38 Kb) - Free access
Bone marrow transplantation as treatment for X-linked immunodeficiency with hyper-IgM.
|Published in||Bone marrow transplantation. 1998, vol. 22, no. 11, p. 1111-4|
|Abstract||We report a 10-year-old boy with a severe form of immunodeficiency with hyper-IgM who underwent successful bone marrow transplantation with his HLA-matched sister as donor. Busulfan (20 mg/kg) and cyclophosphamide (200 mg/kg) were used as conditioning. The post-transplant course was uneventful. He is alive 25 months later with full hematological and immunological reconstitution.|
|Keywords||B-Lymphocytes/immunology — Bone Marrow Transplantation — CD40 Ligand — Child — Chimera/genetics — Female — Genetic Linkage — Humans — Hypergammaglobulinemia/genetics/therapy — Immunoglobulin M/blood — Immunologic Deficiency Syndromes/genetics/therapy — Male — Membrane Glycoproteins/deficiency/genetics — Point Mutation — T-Lymphocytes/immunology — Transplantation, Homologous — X Chromosome/genetics|
|BORDIGONI, P et al. Bone marrow transplantation as treatment for X-linked immunodeficiency with hyper-IgM. In: Bone marrow transplantation, 1998, vol. 22, n° 11, p. 1111-4. doi: 10.1038/sj.bmt.1701497 https://archive-ouverte.unige.ch/unige:74619|