Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome (HHH) Presenting With Acute Fulminant Hepatic Failure-Reference-Cited by-同舟云学术

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Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome (HHH) Presenting With Acute Fulminant Hepatic Failure

Published:2008-03 Issue:3 Volume:46 Page:312-315
ISSN:0277-2116
Container-title:Journal of Pediatric Gastroenterology & Nutrition
language:en
Short-container-title:

Author:

Mhanni AA,Chan A,Collison M,Seifert B,Lehotay DC,Sokoro AH,Huynh HQ,Greenberg CR

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Pediatrics, Perinatology, and Child Health

Reference9 articles.

1. Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia;Hommes;J Inherit Metab Dis,1982

2. Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter;Camacho;Nat Genet,1999

3. A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria;Rodes;J Inherit Metab Dis,1987

4. Clinical and molecular findings in hyperornithinaemia–hyperammonaemia–homocitrullinuria syndrome;Salvi;Neurology,2001

5. HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation;Fecarotta;J Inherit Metab Dis,2006

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Disorders of vesicular trafficking presenting with recurrent acute liver failure: NBAS, RINT1, and SCYL1 deficiency;Journal of Inherited Metabolic Disease;2024-01-27

2. Late onset hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome, presenting as recurrent metabolic encephalopathy, A case report;Annals of Medicine & Surgery;2022-12

3. Role of early management of hyperornithinaemia‐hyperammonaemia‐homocitrullinuria syndrome in pregnancy;BMJ Case Reports;2021-07

4. The Association between SLC25A15 Gene Polymorphisms and Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome: Using In Silico Analysis;2019-09-30

5. Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision;Journal of Inherited Metabolic Disease;2019-05-15

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