67 top medical experts on Succinyl-CoA:3-oxoacid CoA transferase deficiency across 8 countries, including 2 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Succinyl-CoA:3-oxoacid CoA transferase deficiency: A rare, genetic disorder in ketone body utilization characterized by severe, potentially fatal intermittent episodes of ketoacidosis.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- 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: 3-Oxoacid Coa Transferase Deficiency, Ketoacidosis due to SCOT deficiency, SCOT deficiency, Succinyl-Coa 3-Oxoacid Transferase Deficiency, Succinyl-Coa:3-Ketoacid Coa Transferase Deficiency, Succinyl-Coa:3-Ketoacid Coa-Transferase Deficiency, Succinyl-Coa:Acetoacetate Transferase Deficiency
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