Ketoacidotic crisis after vaccination in a girl with beta-ketothiolase deficiency: a case report

Beta-ketothiolase (mitochondrial acetoacetyl-CoA thiolase, T2) is a rare autosomal recessive disease caused by ACAT1 gene pathogenic variant involving isoleucine catabolism and ketone body metabolism disorder. The onset of ketoacidotic crisis commonly follows prior concurrent diseases or triggers in...

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Detalles Bibliográficos
Autores principales: Mao, Shujiong, Yang, Lili, Yin, Xiaoshan, Yang, Jianbin, Huang, Xinwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944172/
https://www.ncbi.nlm.nih.gov/pubmed/33708533
http://dx.doi.org/10.21037/tp-20-265

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944172/
https://www.ncbi.nlm.nih.gov/pubmed/33708533
http://dx.doi.org/10.21037/tp-20-265

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