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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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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 |