Successful liver transplantation in hyperornithinemia‐hyperammonemia‐homocitrullinuria syndrome: Case report-Reference-Cited by-同舟云学术

Successful liver transplantation in hyperornithinemia‐hyperammonemia‐homocitrullinuria syndrome: Case report

Published:2020-12-14 Issue:6 Volume:25 Page:
ISSN:1397-3142
Container-title:Pediatric Transplantation
language:en
Short-container-title:Pediatr Transplant

Author:

De Bruyne Pauline¹^ORCID,Verloo Patrick²^ORCID,Van Hove Johan L. K.³,Hemptinne Bernard⁴,Vande Velde Saskia⁵^ORCID,Van Winckel Myriam⁵^ORCID,Van Biervliet Stephanie⁵^ORCID,De Bruyne Ruth⁵^ORCID

Affiliation:

1. Department of Internal Medicine and Genetics Ghent University Ghent Belgium

2. Department of Pediatric Neurology Princess Elisabeth Children’s Hospital Ghent University Hospital Ghent Belgium

3. Department of Pediatrics University Hospital Gasthuisberg University of Leuven Leuven Belgium

4. Department of General, Hepatobiliary and Liver Transplantation Surgery Ghent University Hospital Ghent Belgium

5. Department of Pediatric Gastroenterology, Hepatology and Nutrition Princess Elisabeth Children’s Hospital Ghent University Hospital Ghent Belgium

Publisher

Wiley

Subject

Transplantation,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/petr.13943

Reference22 articles.

1. Identification of novel mutations in theSLC25A15gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular, and functional study

2. Hyperornithinemia, hyperammonemia, homocitrullinuria (HHH) syndrome: presentation as acute liver disease with coagulopathy;Smith L;J Pediatr Gastroenterol Nutrit,1992

3. Hyperornithinaemia‐hyperammonaemia‐homocitrullinuria syndrome: a treatable genetic liver disease warranting urgent diagnosis;Lee HHC;Hong Kong Med J,2014

4. The hyperornithinemia–hyperammonemia-homocitrullinuria syndrome

5. Insights into the Mutation-Induced HHH Syndrome from Modeling Human Mitochondrial Ornithine Transporter-1

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