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Anesthetic management of a pediatric patient with arginase-1 deficiency undergoing strabismus operation: a case report

BACKGROUND: Urea cycle disorders are rare; arginase-1 deficiency is one of those extremely rare autosomal recessive metabolic disorders. Arginase-1 is one among the enzymes involved in the production of urea from ammonia in the liver, and its deficiency produces the characteristic feature, hyperargi...

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Detalles Bibliográficos
Autores principales: Kato, Hideya, Kawaguchi, Ken, Sawa, Teiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6967156/
https://www.ncbi.nlm.nih.gov/pubmed/32025996
http://dx.doi.org/10.1186/s40981-019-0274-6