10 top medical experts on Liver Glycogen Storage Disease 0 across 1 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Liver Glycogen Storage Disease 0: A genetically inherited anomaly of glycogen metabolism and a form of glycogen storage disease (GSD) characterized by fasting hypoglycemia. This is not a glycogenosis, strictly speaking, as the enzyme deficiency decreases glycogen reserves.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- Association for Glycogen Storage Disease
1542 Flammang Dr.
PMB 1004
Waterloo, IA 50702
E-mail: info@agsdus.org
Website: https://www.agsdus.org/
- Association for Glycogen Storage Disease UK (AGSD-UK)
PO Box 1232
Bristol
BS48 9DD
United Kingdom
Telephone: 0300 123 2790
E-mail: https://agsd.org.uk/contact/message-us2/
Website: http://www.agsd.org.uk/
- Children's Fund for Glycogen Storage Disease Research, Inc.
20 Sherwood Lane
Cheshire, CT 06410
Telephone: 203-272-7744
E-mail: info@curegsd.org
Website: http://www.cureGSD.org
- Metabolic Support UK
5 Hilliards Court
Sandpiper Way
Chester Business Park
Chester, CH4 9QP United Kingdom
Toll-free: 0800 652 3181
Telephone: 0845 241 2173
E-mail: https://www.metabolicsupportuk.org/contact-us
Website: https://www.metabolicsupportuk.org
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- Synonyms: Hypoglycemia With Deficiency Of Glycogen Synthetase In The Liver, Liver Glycogen Synthase Deficiency
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