Infantile hypotonia with failure to thrive

Abstract

BACKGROUND Pompe disease is a lysosomal glycogen storage disease (GSDII) characterized by deficiency of acid glucosidase, resulting in lysosomal glycogen accumulation in multiple tissues, with cardiac and skeletal muscles being the most seriously affected. It manifests itself as a spectrum in multiple age groups including infancy, childhood and adulthood… (More)
DOI: 10.12659/AJCR.883367

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Cite this paper

@inproceedings{Nagiub2012InfantileHW, title={Infantile hypotonia with failure to thrive}, author={Mohamed Nagiub and Karen Alton and Premchand Anne}, booktitle={The American journal of case reports}, year={2012} }