Management of late onset urea cycle disorders—a remaining challenge for the intensivist?

BACKGROUND: Hyperammonemia caused by a disorder of the urea cycle is a rare cause of metabolic encephalopathy that may be underdiagnosed by the adult intensivists because of its rarity. Urea cycle disorders are autosomal recessive diseases except for ornithine transcarbamylase deficiency (OTCD) that...

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Detalles Bibliográficos
Autores principales: Redant, S., Empain, A., Mugisha, A., Kamgang, P., Attou, R., Honoré, P. M., De Bels, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788146/
https://www.ncbi.nlm.nih.gov/pubmed/33409766
http://dx.doi.org/10.1186/s13613-020-00797-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788146/
https://www.ncbi.nlm.nih.gov/pubmed/33409766
http://dx.doi.org/10.1186/s13613-020-00797-y

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