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Understanding Fabry Disease

https://phc.eduhealth.ca/en/permalink/phem2987
Catalogue Number
FA.500.F33
Current Revision Date
February-18-2020
Language
English
Status
Available
Description
Patient information describing this inherited metabolic disorder.

  1 document

Catalogue Number
FA.500.F33
Current Revision Date
February-18-2020
Language
English
Status
Available
Description
Patient information describing this inherited metabolic disorder.
Format
Booklet
Topic
Symptoms, Diseases & Conditions
Procedures, Treatments & Tests
Subject
Metabolic Disorders
Keywords
Metabolic disorders
enzyme deficiency
kidney problems
heart problems
pain
corneal whorling
stomach problems
skin lesion
fatigue
enzyme replacement therapy
lack of sweating
lysosomes
genetic testing
Reading Level
10
Date Issued
November-22-2016
Documents
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Understanding Gaucher Disease

https://phc.eduhealth.ca/en/permalink/phem2988
Catalogue Number
FA.500.G38
Current Revision Date
February-20-2014
Language
English
Status
Available
Description
Patient information describing this inherited metabolic disorder.

  1 document

Catalogue Number
FA.500.G38
Current Revision Date
February-20-2014
Language
English
Status
Available
Description
Patient information describing this inherited metabolic disorder.
Format
Booklet
Topic
Symptoms, Diseases & Conditions
Procedures, Treatments & Tests
Subject
Metabolic Disorders
Keywords
metabolic diseases
lysosomal storage disorders
Inherited disorder
enzyme replacement therapy
spleen problems
liver problems
lung problems
bone problems
Type 1 Gaucher Disease
Type 2 Gaucher Disease
Type 3 Gaucher Disease
genetic testing
substrate reduction therapy
Reading Level
9
Date Issued
November-22-2013
Documents
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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).

  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
Less detail