Skip header and navigation
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
Available
Description
Patient ifnformation on a genetic disorder that is caused by the absence or low levels of the lysosomal enzyme- acid alpha-glucosidase (GAA).
More detail

  1 document

Catalogue Number
FA.500.U53
Current Revision Date
November-25-2015
Language
English
Status
Available
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
Documents
thumbnail

FA.500.U53.pdf

Read PDF Download PDF
Less detail