Glycogen storage disease 0

Common Name(s)

Glycogen storage disease 0

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Glycogen storage disease 0" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Glycogen storage disease 0" returned 3 free, full-text research articles on human participants. First 3 results:

A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0.
 

Author(s): Ana Priscila Soggia, Maria Lúcia Correa-Giannella, Maria Angela Henriques Fortes, Ana Mercedes Cavaleiro Luna, Maria Adelaide Albergaria Pereira

Journal:

 

Glycogen storage disease type 0 is an autosomal recessive disease presenting in infancy or early childhood and characterized by ketotic hypoglycemia after prolonged fasting and postprandial hyperglycemia and hyperlactatemia. Sixteen different mutations have been identified to date ...

Last Updated: 12 Mar 2010

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Cardiomyopathy and exercise intolerance in muscle glycogen storage disease 0.
 

Author(s): Gittan Kollberg, Már Tulinius, Thomas Gilljam, Ingegerd Ostman-Smith, Gun Forsander, Peter Jotorp, Anders Oldfors, Elisabeth Holme

Journal: N. Engl. J. Med.. 2007 Oct;357(15):1507-14.

 

Storage of glycogen is essential for glucose homeostasis and for energy supply during bursts of activity and sustained muscle work. We describe three siblings with profound muscle and heart glycogen deficiency caused by a homozygous stop mutation (R462-->ter) in the muscle glycogen ...

Last Updated: 11 Oct 2007

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Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0.
 

Author(s): M Orho, N U Bosshard, N R Buist, R Gitzelmann, A Aynsley-Green, P Blümel, M C Gannon, F Q Nuttall, L C Groop

Journal: J. Clin. Invest.. 1998 Aug;102(3):507-15.

 

Glycogen storage disease type 0 (GSD-0) is a rare form of fasting hypoglycemia presenting in infancy or early childhood and accompanied by high blood ketones and low alanine and lactate concentrations. Although feeding relieves symptoms, it often results in postprandial hyperglycemia ...

Last Updated: 26 Aug 1998

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Reviews from the PubMed Database

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The terms "Glycogen storage disease 0" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Sleep and Quality of Life in Patients With Glycogen Storage Disease on Standard Versus Modified Uncooked Cornstarch
 

Status: Recruiting

Condition Summary: Glycogen Storage Disease Type IA; Glycogen Storage Disease Type IB; Glycogen Storage Disease Type III; Glycogen Storage Disease Type 0

 

Last Updated: 3 Feb 2014

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