Glycogen storage disease type I: 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 I (patient information)|here]]'''


'''For patient information click [[Glycogen storage disease type I (patient information)|here]]'''
{{DiseaseDisorder infobox |
  Name          = Glycogen storage disease type I |
  ICD10          = {{ICD10|E|74|0|e|70}} |
  ICD9          = {{ICD9|271.0}} |
  ICDO          = |
  Image          = |
  Caption        = |
  OMIM          = 232200 |
  MedlinePlus    = 000338 |
  DiseasesDB    = 5284 |
}}
{{Glycogen storage disease type I}}
{{Glycogen storage disease type I}}
{{CMG}}; {{AE}}{{Anmol}}
{{CMG}}; {{AE}}{{Anmol}}


{{SK}} Glucose-6-phosphatase deficiency; Glycogen storage disease type 1; Glycogenosis type 1; Von Gierke's disease; GSD 1; GSD type 1; Hepatorenal form of GSD; Hepatorenal glycogenosis.
{{SK}} Glucose-6-phosphatase deficiency; Glycogen storage disease type 1; Glycogenosis type 1; von Gierke's disease; GSD type 1; Hepatorenal form of GSD; Hepatorenal glycogenosis


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


==Treatment==
==Treatment==

Latest revision as of 19:33, 6 March 2018


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

Glycogen storage disease type I Microchapters

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Patient Information

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

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X Ray

CT

MRI

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

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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: Glucose-6-phosphatase deficiency; Glycogen storage disease type 1; Glycogenosis type 1; von Gierke's disease; GSD type 1; Hepatorenal form of GSD; Hepatorenal glycogenosis

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

Diagnostoc Study of Choice | History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | X Ray | CT | MRI | 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


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