Find Expert Doctors on 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency135 top medical experts on 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency across 14 countries and 2 U.S. states, including 5 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency: A rare organic aciduria, due to deficiency of 3-hydroxy-3-methylglutaryl-CoA lyase characterized by episodes of metabolic decompensation with hypoketotic hypoglycemia triggered by periods of fasting or infections.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- FOD (Fatty Oxidation Disorder) Family Support Group
P.O. Box 54
Okemos, MI 48805-0054
Telephone: +1-517-381-1940 [8am - 8pm EST every day]
Fax: +1-866-290-5206
E-mail: deb@fodsupport.org
Website: https://fodsupport.org/
- Genetic Metabolic Dietitians International
P.O. Box 1462
Hillsborough, NC 27278
E-mail: info@gdmi.org
Website: http://www.gmdi.org/
- Organic Acidemia Association
9040 Duluth Street
Golden Valley, MN 55427
Telephone: 763-559-1797
Fax: 866-539-4060
E-mail: mkstagni@gmail.com
Website: http://www.oaanews.org/
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- Synonyms: 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency, 3-Hydroxyl 3-Methyl Glutaric Aciduria, Deficiency of Hydroxymethylglutaryl-CoA Lyase, HMG CoA Lyase Deficiency, HMG-CoA Lyase Deficiency, Hydroxymethylglutaric Aciduria
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