Genetic background and clinical characteristics of infantile hyperammonemia
- PMID: 37305718
- PMCID: PMC10248927
- DOI: 10.21037/tp-22-359
Genetic background and clinical characteristics of infantile hyperammonemia
Abstract
Background: This study was conducted to analyze the genetic spectrum and clinical characteristics of infantile hyperammonemia.
Methods: Between January 2016 and June 2020, we retrospectively enrolled infantile hyperammonemia patients with definitive genetic diagnosis at the Children's Hospital of Fudan University. Based on the age of hyperammonemia onset, patients were grouped into neonatal and post-neonatal subgroups to compare their genetic and clinical features.
Results: Collectively, 136 pathogenic or likely pathogenic variants of the 33 genes were identified. Fourteen genes were reported with hyperammonemia (42%, 14/33), with SLC25A13 and MUT being the top two detected genes. In contrast, 19 genes, which have not been previously reported with hyperammonemia, were detected (58%, 19/33), in which JAG1 and ABCC8 were the most frequently mutated genes. Compared with post-neonatal hyperammonemia, neonatal patients with hyperammonemia presented with higher rates of organic acidemia (P=0.001) and fatty acid oxidation disorder (P=0.006), but a lower rate of cholestasis (P<0.001). Patients with neonatal hyperammonemia had a higher ratio of peak plasma ammonia level ≥500 µmol/L (P=0.003) and were more likely to receive precision medicine (P=0.027); however, they had a refractory clinical course (P=0.001) and poorer prognosis than the infantile group.
Conclusions: There were significant differences in the genetic spectrum, clinical features, clinical course, and outcomes between infants with different hyperammonemia onset ages.
Keywords: Genetics; hyperammonemia; infants; neonates.
2023 Translational Pediatrics. All rights reserved.
Conflict of interest statement
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://tp.amegroups.com/article/view/10.21037/tp-22-359/coif). The authors have no conflicts of interest to declare.
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Comment in
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Hyperammonemia and inborn errors of metabolism.Transl Pediatr. 2024 Feb 29;13(2):200-202. doi: 10.21037/tp-23-593. Epub 2024 Feb 26. Transl Pediatr. 2024. PMID: 38455740 Free PMC article. No abstract available.
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