Neurological outcome of patients with ornithine carbamoyltransferase deficiency

Background: Ornithine carbamoyltransferase (OCT) deficiency is the commonest of the inherited urea cycle disorders. Aims: To determine the long term neurological and cognitive outcome of continuously treated surviving patients. Methods: Twenty eight surviving children (five boys) with OCT deficiency...

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Bibliographic Details
Main Authors: Nicolaides, P, Liebsch, D, Dale, N, Leonard, J, Surtees, R
Format: Artigo
Language:Inglês
Published: 2002
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Original Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1719070/
https://ncbi.nlm.nih.gov/pubmed/11806886
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/adc.86.1.54
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