Glycogen storage disease type I: Difference between revisions
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{{SK}} Glucose-6-phosphatase deficiency; glycogen storage disease type 1a; glycogenosis type 1a; von Gierke disease | {{SK}} Glucose-6-phosphatase deficiency; glycogen storage disease type 1a; glycogenosis type 1a; von Gierke disease |
Revision as of 19:20, 19 July 2016
Glycogen storage disease type I Microchapters |
Differentiating Glycogen storage disease type I from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Glycogen storage disease type I On the Web |
American Roentgen Ray Society Images of Glycogen storage disease type I |
Directions to Hospitals Treating Glycogen storage disease type I |
Risk calculators and risk factors for Glycogen storage disease type I |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
For patient information click here Template:DiseaseDisorder infobox
Glycogen storage disease type I Microchapters |
Differentiating Glycogen storage disease type I from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Glycogen storage disease type I On the Web |
American Roentgen Ray Society Images of Glycogen storage disease type I |
Directions to Hospitals Treating Glycogen storage disease type I |
Risk calculators and risk factors for Glycogen storage disease type I |
Synonyms and keywords: Glucose-6-phosphatase deficiency; glycogen storage disease type 1a; glycogenosis type 1a; von Gierke disease
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Glycogen storage disease type I from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | X Ray | CT | MRI |Ultrasound | Other Image Findings | Other Diagnostic Studies
Treatment
Dietary Therapy | Medical Therapy | Surgery | Primary Prevention | Primary Prevention |Cost-Effectiveness of Therapy | Future or Investigational Therapies