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Patient Health Education Materials

Understanding Late-Onset Pompe Disease

https://phc.eduhealth.ca/en/permalink/phem3287
Catalogue Number
FA.500.U53
Current Revision Date
November-25-2015
Language
English
Status
Pending or under revision
Description
Patient ifnformation on a genetic disorder that is caused by the absence or low levels of the lysosomal enzyme- acid alpha-glucosidase (GAA).
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Catalogue Number
FA.500.U53
Current Revision Date
November-25-2015
Language
English
Status
Pending or under revision
Description
Patient ifnformation on a genetic disorder that is caused by the absence or low levels of the lysosomal enzyme- acid alpha-glucosidase (GAA).
Format
Booklet
Topic
Symptoms, Diseases & Conditions
Procedures, Treatments & Tests
Subject
Metabolic Disorders
Keywords
lysosomal storage disorders
Glycogen Storage Disorders
muscle weakness
breathing difficulties
genetic disease
enzyme replacement therapy
Reading Level
9
Date Issued
November-19-2015
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