期刊
JOURNAL OF INHERITED METABOLIC DISEASE
卷 27, 期 5, 页码 691-692出版社
KLUWER ACADEMIC PUBL
DOI: 10.1023/B:BOLI.0000043023.57321.18
关键词
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SCOT deficiency presents with persistent excess of ketones leading to ketoacidosis. Here we report patient GS15, homozygous for a novel R217X mutation, who had the first apparent ketoacidotic crisis at 8 months of age. Before confirmation of diagnosis, daily dialysis was the only mechanism by which to normalize her persistent metabolic acidosis of unknown aetiology.
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