Headache: A Presentation of Pompe Disease; A Case Report
Pompe disease, also termed glycogen storage disease type II or acid maltase deficiency, caused by deficient activity of acid alpha-glucosidase (GAA), the glycogen degrading lysosomal enzyme. As a result, massive lysosomal glycogen deposits in the numerous organs including the muscles. In Pompe disea...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Guilan University of Medical Sciences
2017-02-01
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| Series: | Caspian Journal of Neurological Sciences |
| Subjects: | |
| Online Access: | http://cjns.gums.ac.ir/browse.php?a_code=A-10-32-66&slc_lang=en&sid=1 |