Acute treatment of hyperammonemia by continuous renal replacement therapy in a newborn patient with ornithine transcarbamylase deficiency

Ornithine transcarbamylase (OTC) deficiency is well known as the most common inherited disorder of the urea cycle, and 1 of the most common causes of hyperammonemia in newborns. We experienced a case of a 3-day-old boy with OTC deficiency who appeared healthy in the first 2 days of life but develope...

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Detalhes bibliográficos
Main Authors: Kim, Hyo Jeong, Park, Se Jin, Park, Kook In, Lee, Jin Sung, Eun, Ho Sun, Kim, Ji Hong, Shin, Jae Il
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Pediatric Society 2011
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3250597/
https://ncbi.nlm.nih.gov/pubmed/22232626
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2011.54.10.425
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