Literature DB >> 7155674

Liver peroxisome damage during acute hepatic failure in partial ornithine transcarbamylase deficiency.

P Landrieu, B François, G Lyon, F Van Hoof.   

Abstract

A boy with ornithine transcarbamylase (OTC) deficiency was relatively symptom free for 9 months and then developed an acute episode with liver failure and metabolic imbalance. Subsequently there was severe cerebral atrophy. Liver ornithine transcarbamylase activity was 3% of the normal mean. Of considerable interest was the finding of an accelerated breakdown of liver peroxisomes during the acute phase.

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Year:  1982        PMID: 7155674     DOI: 10.1203/00006450-198212000-00001

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  5 in total

Review 1.  Secondary alterations of human hepatocellular peroxisomes.

Authors:  D De Craemer
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

2.  Hepatocellular carcinoma in a research subject with ornithine transcarbamylase deficiency.

Authors:  James M Wilson; Oleg A Shchelochkov; Renata C Gallagher; Mark L Batshaw
Journal:  Mol Genet Metab       Date:  2011-11-07       Impact factor: 4.797

3.  Significant hepatic involvement in patients with ornithine transcarbamylase deficiency.

Authors:  Renata C Gallagher; Christina Lam; Derek Wong; Stephen Cederbaum; Ronald J Sokol
Journal:  J Pediatr       Date:  2014-01-30       Impact factor: 4.406

4.  Late onset ornithine carbamoyl transferase deficiency in males.

Authors:  E Drogari; J V Leonard
Journal:  Arch Dis Child       Date:  1988-11       Impact factor: 3.791

5.  Protection of rats by clofibrate against the hypoglycaemic and toxic effects of hypoglycin and pent-4-enoate. An ultrastructural and biochemical study.

Authors:  F Van Hoof; L Hue; J Vamecq; H S Sherratt
Journal:  Biochem J       Date:  1985-07-15       Impact factor: 3.857

  5 in total

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