Skeletal muscle pathology of infantile Pompe disease during long-term enzyme replacement therapy

Sean N. Prater, Trusha Patel, Anne F. Buckley, Hanna Mandel, Eugene Vlodavski, Suhrad G. Banugaria, Erin Feeney, Nina Raben, Priya S. Kishnani

Orphanet Journal of Rare Diseases · 2013 · 80 citations · 32 references

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Abstract

This is the first study to investigate the impact of rhGAA ERT on lysosomal glycogen accumulation and autophagic buildup in patients with classic IPD beyond 18 months of treatment. Our findings indicate that ERT does not fully halt or reverse the underlying skeletal muscle pathology in IPD. The best outcomes were observed in the two patients who began therapy early, namely at 0.5 and 1.1 months of age.

References

32