Article
T-cell-depleted peripheral blood stem cell transplantation for alpha-mannosidosis.
Bone marrow transplantation - 1 Aug 2003
Albert M H, Schuster F, Peters C, Schulze S, Pontz B F, Muntau A C, Röschinger W, Stachel D K, Enders A, Haas R J, Schmid I
Abstract excerpt
Alpha-mannosidosis (alpha-mannosidosis) is a lysosomal storage disease characterized by accumulation of oligosaccharides in various tissues leading to symptoms such as coarse facial features, dysostosis multiplex, hearing disabilities, mental developmental delay and skeletal involvement (dysostosis multiplex). Without treatment, the severe infantile onset form of this autosomal recessive disease leads to...
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