Glycogen storage disease type II: Difference between revisions
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{{SK}} Glycogen storage disease type II; Pompe disease; acid maltase deficiency; glycogenosis type 2; alpha-1, 4-glucosidase deficiency{{Glycogen storage disease type II}} | |||
{{SK}} Glycogen storage disease type II; Pompe disease; acid maltase deficiency; glycogenosis type 2; alpha-1, 4-glucosidase deficiency | |||
==[[Glycogen storage disease type II overview|Overview]]== | ==[[Glycogen storage disease type II overview|Overview]]== |
Revision as of 17:51, 5 January 2018
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Glycogen storage disease type II | |
ICD-10 | E74.0 |
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ICD-9 | 271.0 |
OMIM | 232300 |
DiseasesDB | 5296 |
MeSH | D006009 |
Synonyms and keywords: Glycogen storage disease type II; Pompe disease; acid maltase deficiency; glycogenosis type 2; alpha-1, 4-glucosidase deficiency
Glycogen storage disease type II Microchapters |
Differentiating Glycogen storage disease type II from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Glycogen storage disease type II On the Web |
American Roentgen Ray Society Images of Glycogen storage disease type II |
Directions to Hospitals Treating Glycogen storage disease type II |
Risk calculators and risk factors for Glycogen storage disease type II |
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 | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
Case Studies
Case #1 it:morbo di Pompe de:Morbus Pompe