An incidental finding in newborn screening leading to the diagnosis of a patient with ECHS1 mutations

Short-chain enoyl-CoA hydratase (ECHS1) is a mitochondrial beta-oxidation enzyme involved in the metabolism of acyl-CoA fatty acid esters, as well as in valine metabolism. ECHS1 deficiency has multiple manifestations, including Leigh syndrome early at birth or in childhood with poor prognosis, to cu...

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Detalles Bibliográficos
Autores principales: Pajares, S., López, R.M., Gort, L., Argudo-Ramírez, A., Marín, J.L., González de Aledo-Castillo, J.M., García-Villoria, J., Arranz, J.A., Del Toro, M., Tort, F., Ugarteburu, O., Casellas, M.D., Fernández, R., Ribes, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940607/
https://www.ncbi.nlm.nih.gov/pubmed/31908952
http://dx.doi.org/10.1016/j.ymgmr.2019.100553

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940607/
https://www.ncbi.nlm.nih.gov/pubmed/31908952
http://dx.doi.org/10.1016/j.ymgmr.2019.100553

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