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Bone marrow transplantation as treatment for X-linked immunodeficiency with hyper-IgM

Bone Marrow Transplantation volume 22, pages 1111–1114 (1998)Cite this article

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.

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Authors and Affiliations

  1. Bone Marrow Transplantation Unit, Children’s Hospital, Nancy, Paris, France

    P Bordigoni, B Auburtin, A-S Carret, A Schuhmacher, J-C Humbert & D Sommelet

  2. INSERM U 429, Hôpital Necker, Paris, France

    F Le Deist

Authors
  1. P Bordigoni
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  2. B Auburtin
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  3. A-S Carret
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  4. A Schuhmacher
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  5. J-C Humbert
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  6. F Le Deist
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  7. D Sommelet
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Bordigoni, P., Auburtin, B., Carret, AS. et al. Bone marrow transplantation as treatment for X-linked immunodeficiency with hyper-IgM. Bone Marrow Transplant 22, 1111–1114 (1998). https://doi.org/10.1038/sj.bmt.1701497

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  • DOI: https://doi.org/10.1038/sj.bmt.1701497

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