Glycogen storage disease type III: Difference between revisions
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'''For the main page on glycogen storage disease, please click [[Glycogen storage disease|here]]'''<br> | |||
'''For patient information click [[Glycogen storage disease type III (patient information)|here]]''' | |||
{{Glycogen storage disease type III}} | {{Glycogen storage disease type III}} | ||
{{CMG}}; {{AE}}{{Anmol}} | {{CMG}}; {{AE}}{{Anmol}} | ||
{{SK}} Glycogen storage disease type 3; GSD type 3; GSD 3; Cori disease; Forbes disease; limit dextrinosis; glycogenosis type 3; amylo-1, 6-glucosidase deficiency; debrancher enzyme deficiency; glycogen debranching enzyme deficiency; AGL deficiency; GDE deficiency; 4-alpha-glucanotransferase enzyme deficiency. | {{SK}} Glycogen storage disease type 3; GSD type 3; GSD 3; Cori disease; Forbes disease; limit dextrinosis; glycogenosis type 3; amylo-1, 6-glucosidase deficiency; debrancher enzyme deficiency; glycogen debranching enzyme deficiency; AGL deficiency; GDE deficiency; 4-alpha-glucanotransferase enzyme deficiency. | ||
==[[Glycogen storage disease type III overview|Overview]]== | ==[[Glycogen storage disease type III overview|Overview]]== |
Latest revision as of 18:04, 31 January 2018
For the main page on glycogen storage disease, please click here
For patient information click here
Glycogen storage disease type III Microchapters |
Differentiating Glycogen storage disease type III from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Glycogen storage disease type III On the Web |
American Roentgen Ray Society Images of Glycogen storage disease type III |
Risk calculators and risk factors for Glycogen storage disease type III |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]
Synonyms and keywords: Glycogen storage disease type 3; GSD type 3; GSD 3; Cori disease; Forbes disease; limit dextrinosis; glycogenosis type 3; amylo-1, 6-glucosidase deficiency; debrancher enzyme deficiency; glycogen debranching enzyme deficiency; AGL deficiency; GDE deficiency; 4-alpha-glucanotransferase enzyme deficiency.
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Glycogen Storage Disease Type III from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic study of choice | History and Symptoms | Physical Examination | Electrocardiogram | Laboratory Findings | X-Ray Findings | Echocardiography and Ultrasound | CT-Scan Findings | MRI Findings | Other Diagnostic Studies | Other Imaging Findings
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies