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Deficiencia de succinil-CoA acetoacetato transferasa: reporte de un caso
BACKGROUND: Succinyl-CoA:3 oxoacid CoA transferase deficiency (SCOTD) is a rare autosomal recessive disease, characterized by altered utilization of ketone bodies, with acute episodes of ketoacidosis. CLINICAL CASE: It is presented the case of a patient with SCOTD, with a first atypical episode acco...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Instituto Mexicano del Seguro Social
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599782/ https://www.ncbi.nlm.nih.gov/pubmed/37773183 http://dx.doi.org/10.5281/zenodo.8316483 |