Literature DB >> 16601889

HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation.

S Fecarotta1, G Parenti, P Vajro, A Zuppaldi, R Della Casa, M T Carbone, A Correra, G Torre, S Riva, C Dionisi-Vici, F M Santorelli, G Andria.   

Abstract

We report a 3-year-old Italian patient with the hyperornithinaemia, hyperammonaemia, homocitrullinuria (HHH) syndrome who presented with neurological deterioration after an intercurrent infection. Hyperammonaemia, coagulopathy and moderate hypertransaminasaemia were detected on hospital admission. Severe hepatocellular necrosis with hypertransaminasaemia (aspartate aminotransferase 20,000 UI/L, alanine aminotransferase 18,400 UI/L) and coagulopathy (PT < 5%) rapidly developed within few days, prompting evaluation for liver transplantation. A protein-restricted diet and arginine supplementation were immediately started, with a rapid improvement of the patient's neurological conditions and normalization of liver function tests and blood ammonia. The diagnosis of HHH syndrome was based on the presence of the typical metabolic abnormalities. Molecular analysis of the SLC25A15 gene showed that the patient was heterozygous for two novel mutations (G113C and M273K). The diagnosis of HHH syndrome should be considered in patients with fulminant hepatitis-like presentations. Early identification and treatment of these patients can be life-saving and can avoid liver transplantation.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16601889     DOI: 10.1007/s10545-006-0120-7

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  12 in total

1.  A COLORIMETRIC DETERMINATION OF OROTIC ACID.

Authors:  T ADACHI; A TANIMURA; M ASAHINA
Journal:  J Vitaminol (Kyoto)       Date:  1963-09-10

2.  A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet.

Authors:  L R Gjessing; H A Lunde; T Undrum; H Broch; A Alme; S O Lie
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.

Authors:  S Salvi; F M Santorelli; E Bertini; R Boldrini; C Meli; A Donati; A B Burlina; C Rizzo; M Di Capua; G Fariello; C Dionisi-Vici
Journal:  Neurology       Date:  2001-09-11       Impact factor: 9.910

4.  Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: low creatine excretion and effect of citrulline, arginine, or ornithine supplement.

Authors:  C Dionisi Vici; C Bachmann; M Gambarara; J P Colombo; G Sabetta
Journal:  Pediatr Res       Date:  1987-09       Impact factor: 3.756

5.  Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter.

Authors:  J A Camacho; C Obie; B Biery; B K Goodman; C A Hu; S Almashanu; G Steel; R Casey; M Lambert; G A Mitchell; D Valle
Journal:  Nat Genet       Date:  1999-06       Impact factor: 38.330

6.  Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia.

Authors:  F A Hommes; C K Ho; R A Roesel; M E Coryell; B A Gordon
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

7.  Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.

Authors:  V E Shih; M L Efron; H W Moser
Journal:  Am J Dis Child       Date:  1969-01

8.  Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome with evidence of mitochondrial dysfunction due to a novel SLC25A15 (ORNT1) gene mutation in a Palestinian family.

Authors:  Stanley H Korman; Naomi Kanazawa; Bassam Abu-Libdeh; Alisa Gutman; Seiichi Tsujino
Journal:  J Neurol Sci       Date:  2004-03-15       Impact factor: 3.181

9.  Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuria.

Authors:  M D Haust; P D Gatfield; B A Gordon
Journal:  Hum Pathol       Date:  1981-03       Impact factor: 3.466

Review 10.  Inborn errors presenting with liver dysfunction.

Authors:  Peter T Clayton
Journal:  Semin Neonatol       Date:  2002-02
View more
  14 in total

1.  Ornithine and Homocitrulline Impair Mitochondrial Function, Decrease Antioxidant Defenses and Induce Cell Death in Menadione-Stressed Rat Cortical Astrocytes: Potential Mechanisms of Neurological Dysfunction in HHH Syndrome.

Authors:  Ângela Zanatta; Marília Danyelle Nunes Rodrigues; Alexandre Umpierrez Amaral; Débora Guerini Souza; André Quincozes-Santos; Moacir Wajner
Journal:  Neurochem Res       Date:  2016-05-09       Impact factor: 3.996

2.  Diagnosis and high incidence of hyperornithinemia-hyperammonemia-homocitrullinemia (HHH) syndrome in northern Saskatchewan.

Authors:  AbdulRazaq A H Sokoro; Joyce Lepage; Nick Antonishyn; Ryan McDonald; Cheryl Rockman-Greenberg; James Irvine; Denis C Lehotay
Journal:  J Inherit Metab Dis       Date:  2010-06-24       Impact factor: 4.982

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.  Ornithine In Vivo Administration Disrupts Redox Homeostasis and Decreases Synaptic Na(+), K (+)-ATPase Activity in Cerebellum of Adolescent Rats: Implications for the Pathogenesis of Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) Syndrome.

Authors:  Ângela Zanatta; Carolina Maso Viegas; Fernanda Hermes Hickmann; Wagner de Oliveira Monteiro; Angela Sitta; Daniela de Moura Coelho; Carmen Regla Vargas; Guilhian Leipnitz; Moacir Wajner
Journal:  Cell Mol Neurobiol       Date:  2015-03-13       Impact factor: 5.046

5.  Heterologous Expression in Yeast of Human Ornithine Carriers ORNT1 and ORNT2 and of ORNT1 Alleles Implicated in HHH Syndrome in Humans.

Authors:  Mara Doimo; Raffaele Lopreiato; Valentina Basso; Raissa Bortolotto; Alessandra Tessa; Filippo M Santorelli; Eva Trevisson; Leonardo Salviati
Journal:  JIMD Rep       Date:  2015-11-21

Review 6.  Suggested guidelines for the diagnosis and management of urea cycle disorders.

Authors:  Johannes Häberle; Nathalie Boddaert; Alberto Burlina; Anupam Chakrapani; Marjorie Dixon; Martina Huemer; Daniela Karall; Diego Martinelli; Pablo Sanjurjo Crespo; René Santer; Aude Servais; Vassili Valayannopoulos; Martin Lindner; Vicente Rubio; Carlo Dionisi-Vici
Journal:  Orphanet J Rare Dis       Date:  2012-05-29       Impact factor: 4.123

7.  Insights into the mutation-induced HHH syndrome from modeling human mitochondrial ornithine transporter-1.

Authors:  Jing-Fang Wang; Kuo-Chen Chou
Journal:  PLoS One       Date:  2012-01-26       Impact factor: 3.240

Review 8.  The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.

Authors:  Diego Martinelli; Daria Diodato; Emanuela Ponzi; Magnus Monné; Sara Boenzi; Enrico Bertini; Giuseppe Fiermonte; Carlo Dionisi-Vici
Journal:  Orphanet J Rare Dis       Date:  2015-03-11       Impact factor: 4.123

9.  Carnitine deficiency presenting with encephalopathy and hyperammonemia in a patient receiving chronic enteral tube feeding: a case report.

Authors:  Peter Ling; Douglas J Lee; Eric M Yoshida; Sandra Sirrs
Journal:  J Med Case Rep       Date:  2012-07-30

10.  A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: functional analysis of the mutant protein.

Authors:  Nagehan Ersoy Tunalı; Carlo M T Marobbio; N Ozan Tiryakioğlu; Giuseppe Punzi; Seha K Saygılı; Hasan Onal; Ferdinando Palmieri
Journal:  Mol Genet Metab       Date:  2014-03-20       Impact factor: 4.797

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.