The effects of early and late bone marrow transplantation in siblings with alpha-mannosidosis. Is early haematopoietic cell transplantation the preferred treatment option?

A. A. Broomfield, A. Chakrapani, J. E. Wraith

    Research output: Contribution to journalArticlepeer-review

    Abstract

    This article documents both the neurological and physical outcomes of the first published set of siblings undergoing transplantation at differing ages for α-mannosidosis. The older brother, the index case, was diagnosed at the age of 3 years and underwent transplantation at 13 years for the treatment of increasing somatic problems and recurrent infections. The younger brother had undergone transplantation pre-symptomatically at 6 months of age. Their clinical, radiological and developmental outcomes are documented and compared with the previous published cases, with the case for early transplantation being weighted against other potential therapies. © SSIEM and Springer 2010.
    Original languageEnglish
    Pages (from-to)S123-S127
    JournalJournal of Inherited Metabolic Disease
    Volume33
    Issue number3
    DOIs
    Publication statusPublished - 2010

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