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Adult Metabolic Diseases Clinic, Welcome to (VGH)

https://vch.eduhealth.ca/en/permalink/phem142
Catalogue Number
FA.502.Ad93
Current Revision Date
June-23-2016
Language
English
Status
Available
Description
Information about Adult Metabolic Disease Clinic at Vancouver General Hospital
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Catalogue Number
FA.502.Ad93
Current Revision Date
June-23-2016
Language
English
Status
Available
Description
Information about Adult Metabolic Disease Clinic at Vancouver General Hospital
Format
Booklet
Topic
Symptoms, Diseases & Conditions
Subject
Nutrition Assessment Services
Metabolic Disorders
Nutrition
Keywords
Metabolic disorders
outpatient
nutrition
counseling
education
Reading Level
0
Date Issued
January-01-2002
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FA.502.Ad93.pdf

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Understanding Carnitine Uptake Disorder (CUD)

https://vch.eduhealth.ca/en/permalink/phem3124
Catalogue Number
GI.300.C37
Current Revision Date
February-18-2020
Language
English
Status
Available
Description
The treatment and management of Carnitine Uptake Disorder
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  1 document

Catalogue Number
GI.300.C37
Current Revision Date
February-18-2020
Language
English
Status
Available
Description
The treatment and management of Carnitine Uptake Disorder
Format
Booklet
Topic
Symptoms, Diseases & Conditions
Subject
Genetic disorders
Keywords
deficiency
heart problems
Fasting
Inherited disorder
Mutation
fatty acid oxidation disorder
blood sugar
liver problems
genetic testing
Metabolic disorders
Reading Level
9
Date Issued
September-02-2014
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GI.300.C37.pdf

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Understanding Fabry Disease

https://vch.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.
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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
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FA.500.F33.pdf

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Understanding Gaucher Disease

https://vch.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.
More detail

  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
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FA.500.G38.pdf

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Understanding Glycogen Storage Disease

https://vch.eduhealth.ca/en/permalink/phem140
Catalogue Number
FA.500.Un22
Language
English
Status
Pending or under revision
Description
Information about Glycogen Storage Disease
More detail
Catalogue Number
FA.500.Un22
Language
English
Status
Pending or under revision
Description
Information about Glycogen Storage Disease
Format
Booklet
Topic
Symptoms, Diseases & Conditions
Healthy Living
Subject
Nutrition Assessment Services
Metabolic Disorders
Nutrition
Keywords
Metabolic disorders
Genetic disorders
von Gierke’s disease
metabolism
hypoglycemia
Reading Level
0
Date Issued
September-22-2006
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Understanding Homocystinuria

https://vch.eduhealth.ca/en/permalink/phem141
Catalogue Number
FA.500.Un23
Language
English
Status
Pending or under revision
Description
Information about Homocystinuria
More detail
Catalogue Number
FA.500.Un23
Language
English
Status
Pending or under revision
Description
Information about Homocystinuria
Format
Booklet
Topic
Symptoms, Diseases & Conditions
Subject
Nutrition Assessment Services
Metabolic Disorders
Nutrition
Keywords
Metabolic disorders
generic disorders
metabolism
nutritional disorder
diets
methionine
Reading Level
0
Date Issued
September-22-2006
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Understanding Late-Onset Pompe Disease

https://vch.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).
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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
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FA.500.U53.pdf

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Understanding Mitochondrial Disorders

https://vch.eduhealth.ca/en/permalink/phem139
Catalogue Number
FA.500.Un21
Current Revision Date
April-12-2017
Language
English
Status
Available
Description
Information about Mitochondrial Disorders
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  1 document

Catalogue Number
FA.500.Un21
Current Revision Date
April-12-2017
Language
English
Status
Available
Description
Information about Mitochondrial Disorders
Format
Booklet
Topic
Symptoms, Diseases & Conditions
Healthy Living
Subject
Nutrition Assessment Services
Metabolic Disorders
Nutrition
Keywords
Metabolic disorders
Genetic disorders
ATP
fatigue
diets
Exercises
Reading Level
10
Date Issued
September-22-2006
Documents
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FA.500.Un21.pdf

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Understanding the CPT 1A Variant - A guide for First Nations People

https://vch.eduhealth.ca/en/permalink/phem2604
Catalogue Number
FA.510.U53
Current Revision Date
February-18-2020
Language
English
Status
Available
Description
Patient information on this rare metabolic disorder discussing symptoms, treatment, diagnosis and pregnancy.
More detail

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Catalogue Number
FA.510.U53
Current Revision Date
February-18-2020
Language
English
Status
Available
Description
Patient information on this rare metabolic disorder discussing symptoms, treatment, diagnosis and pregnancy.
Format
Booklet
Topic
Procedures, Treatments & Tests
Aboriginal Health
People with Chronic Diseases
Symptoms, Diseases & Conditions
Subject
Metabolic Disorders
Keywords
energy
fatty acid oxidation disorder
First Nations
foods
diets
water
alcohol
complications
Reading Level
12
Date Issued
January-19-2012
Documents
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FA.510.U53.pdf

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Understanding Urea Cycle Disorders

https://vch.eduhealth.ca/en/permalink/phem138
Catalogue Number
FA.500.Un2
Language
English
Status
Pending or under revision
Description
Information about Urea Cycle Disorders
More detail
Catalogue Number
FA.500.Un2
Language
English
Status
Pending or under revision
Description
Information about Urea Cycle Disorders
Format
Booklet
Topic
Symptoms, Diseases & Conditions
Subject
Nutrition Assessment Services
Metabolic Disorders
Nutrition
Keywords
Metabolic disorders
Genetic disorders
enzyme deficiency
nutritional disorder
diets
medications
Reading Level
0
Date Issued
September-22-2006
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10 records – page 1 of 1.