Glycogen storage disease type II: 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 II (patient information)|here]]'''
{{Glycogen storage disease type II}}
{{CMG}}; {{AE}}{{Anmol}}  
{{CMG}}; {{AE}}{{Anmol}}  


{{Infobox_Disease |
{{SK}} Glycogen storage disease type 2; Pompe disease; acid maltase deficiency; glycogenosis type 2; alpha-1, 4-glucosidase deficiency; GSD II; GSD type 2; acid alpha-glucosidase deficiency; GAA deficiency; Generalized cardiac form glycogenosis; Cardiomegalia glycogenica diffusa.
  Name          = {{PAGENAME}} |
  Image          = |
  Caption        = |
  DiseasesDB    = 5296 |
  ICD10          = {{ICD10|E|74|0|e|70}} |
  ICD9          = {{ICD9|271.0}} |
  ICDO          = |
  OMIM          = 232300 |
  MedlinePlus    = |
  MeshID        = D006009 |
}}
{{SK}} Glycogen storage disease type II; Pompe disease; acid maltase deficiency; glycogenosis type 2; alpha-1, 4-glucosidase deficiency{{Glycogen storage disease type II}}


==[[Glycogen storage disease type II overview|Overview]]==
==[[Glycogen storage disease type II overview|Overview]]==
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==Diagnosis==
==Diagnosis==
[[Glycogen storage disease type II history and symptoms|History and Symptoms]] | [[Glycogen storage disease type II physical examination|Physical Examination]] | [[Glycogen storage disease type II laboratory findings|Laboratory Findings]] | [[Glycogen storage disease type II electrocardiogram|Electrocardiogram]] | [[Glycogen storage disease type II x ray|X Ray]] | [[Glycogen storage disease type II CT|CT]] | [[Glycogen storage disease type II MRI|MRI]] | [[Glycogen storage disease type II echocardiography or ultrasound|Echocardiography or Ultrasound]] | [[Glycogen storage disease type II other imaging findings|Other Imaging Findings]] | [[Glycogen storage disease type II other diagnostic studies|Other Diagnostic Studies]]
[[Glycogen storage disease type II diagnostic study of choice|Diagnostic study of Choice]] | [[Glycogen storage disease type II history and symptoms|History and Symptoms]] | [[Glycogen storage disease type II physical examination|Physical Examination]] | [[Glycogen storage disease type II laboratory findings|Laboratory Findings]] | [[Glycogen storage disease type II electrocardiogram|Electrocardiogram]] | [[Glycogen storage disease type II x ray|X Ray]] | [[Glycogen storage disease type II CT|CT]] | [[Glycogen storage disease type II MRI|MRI]] | [[Glycogen storage disease type II echocardiography or ultrasound|Echocardiography or Ultrasound]] | [[Glycogen storage disease type II other imaging findings|Other Imaging Findings]] | [[Glycogen storage disease type II other diagnostic studies|Other Diagnostic Studies]]


==Treatment==
==Treatment==
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Latest revision as of 19:58, 4 April 2018


For the main page on glycogen storage disease, please click here
For patient information click here

Glycogen storage disease type II Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Glycogen storage disease type II from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

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

Glycogen storage disease type II On the Web

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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 2; Pompe disease; acid maltase deficiency; glycogenosis type 2; alpha-1, 4-glucosidase deficiency; GSD II; GSD type 2; acid alpha-glucosidase deficiency; GAA deficiency; Generalized cardiac form glycogenosis; Cardiomegalia glycogenica diffusa.

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Glycogen storage disease type II from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic study of Choice | 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


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