Adult onset type II citrullinemia as a cause of non-alcoholic steatohepatitis
- PMID: 16278034
- DOI: 10.1016/j.jhep.2005.08.024
Adult onset type II citrullinemia as a cause of non-alcoholic steatohepatitis
Abstract
Adult onset type II citrullinemia (CTLN2) is an autosomal recessive disease accompanied with hyperammonemia and a sudden onset of psychiatric disorders. We demonstrated three male patients with CTLN2 having a liver histology of non-alcoholic steatohepatitis (NASH). Patients with NASH were analyzed for the causative gene of CTLN2, SLC25A13 and discussed.
Similar articles
-
Citrin deficiency as a cause of chronic liver disorder mimicking non-alcoholic fatty liver disease.J Hepatol. 2008 Nov;49(5):810-20. doi: 10.1016/j.jhep.2008.05.016. Epub 2008 Jun 10. J Hepatol. 2008. PMID: 18620775
-
Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD).J Hum Genet. 2002;47(7):333-41. doi: 10.1007/s100380200046. J Hum Genet. 2002. PMID: 12111366 Review.
-
A case of adult-onset type II citrullinemia--deterioration of clinical course after infusion of hyperosmotic and high sugar solutions.Med Sci Monit. 2006 Feb;12(2):CS13-5. Epub 2006 Jan 26. Med Sci Monit. 2006. PMID: 16449956
-
Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologue.Genomics. 1999 Dec 1;62(2):289-92. doi: 10.1006/geno.1999.6006. Genomics. 1999. PMID: 10610724
-
[Progresses and perspectives in the study on citrin deficiency].Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Dec;23(6):655-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 17160946 Review. Chinese.
Cited by
-
Living Related Liver Transplantation for Metabolic Liver Diseases in Children.J Pediatr Gastroenterol Nutr. 2021 Jan 1;72(1):11-17. doi: 10.1097/MPG.0000000000002952. J Pediatr Gastroenterol Nutr. 2021. PMID: 32969959 Free PMC article.
-
The Lack of Hepatocyte Steatosis in Adult-onset Type II Citrullinemia Patients as Assessed by 7-year Interval Paired Biopsies.Intern Med. 2019 Jul 1;58(13):1891-1895. doi: 10.2169/internalmedicine.2374-18. Epub 2019 Feb 25. Intern Med. 2019. PMID: 30799367 Free PMC article.
-
The impact of solute carrier proteins on disrupting substance regulation in metabolic disorders: insights and clinical applications.Front Pharmacol. 2025 Jan 9;15:1510080. doi: 10.3389/fphar.2024.1510080. eCollection 2024. Front Pharmacol. 2025. PMID: 39850557 Free PMC article. Review.
-
Genetic determinants of hepatic steatosis in man.J Lipid Res. 2011 Apr;52(4):593-617. doi: 10.1194/jlr.R008896. Epub 2011 Jan 18. J Lipid Res. 2011. PMID: 21245030 Free PMC article. Review.
-
Management of late onset urea cycle disorders-a remaining challenge for the intensivist?Ann Intensive Care. 2021 Jan 6;11(1):2. doi: 10.1186/s13613-020-00797-y. Ann Intensive Care. 2021. PMID: 33409766 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical