Clinical and Genetic Spectra of Inherited Liver Disease in Children in China

Background: Children presenting with chronic liver disease or acute liver failure often have an underlying genetic disorder. The aim of this study was to analyze the clinical and genetic spectra of inherited liver disease in children in a tertiary hospital.Methods: A total of 172 patients were class...

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Main Authors: Youhong Fang (Author), Jindan Yu (Author), Jingan Lou (Author), Kerong Peng (Author), Hong Zhao (Author), Jie Chen (Author)
Format: Book
Published: Frontiers Media S.A., 2021-03-01T00:00:00Z.
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001 doaj_89f58b18b45d4c9bb569f061dccecfe9
042 |a dc 
100 1 0 |a Youhong Fang  |e author 
700 1 0 |a Jindan Yu  |e author 
700 1 0 |a Jingan Lou  |e author 
700 1 0 |a Kerong Peng  |e author 
700 1 0 |a Hong Zhao  |e author 
700 1 0 |a Jie Chen  |e author 
245 0 0 |a Clinical and Genetic Spectra of Inherited Liver Disease in Children in China 
260 |b Frontiers Media S.A.,   |c 2021-03-01T00:00:00Z. 
500 |a 2296-2360 
500 |a 10.3389/fped.2021.631620 
520 |a Background: Children presenting with chronic liver disease or acute liver failure often have an underlying genetic disorder. The aim of this study was to analyze the clinical and genetic spectra of inherited liver disease in children in a tertiary hospital.Methods: A total of 172 patients were classified into three groups according to their clinical presentation: cholestasis (Group A), liver enzyme elevation (Group B), and hepato/splenomegaly (Group C). Next-generation sequencing (NGS) was performed on all patients recruited in this study. The genotypic and phenotypic spectra of disease in these patients were reviewed.Results: The median age at enrollment of the 172 patients was 12.0 months (IQR: 4.9, 42.5 months), with 52.3% males and 47.7% females. The overall diagnostic rate was 55.8% (96/172) in this group. The diagnostic rates of whole-exome sequencing (WES) and targeted gene panel sequencing (TGPS) were 47.2% and 62.0%, respectively (no significant difference, p = 0.054). We identified 25 genes related to different phenotypes, including 46 novel disease-related pathogenic mutations. The diagnostic rates in the three groups were 46.0% (29/63), 48.6% (34/70), and 84.6% (33/39). ATP7B, SLC25A13, and G6PC were the top three genes related to monogenic liver disease in this study.Conclusion: WES and TGPS show similar diagnostic rates in the diagnosis of monogenic liver disease. NGS has an important role in the diagnosis of monogenetic liver disease and can provide more precise medical treatment and predict the prognosis of these diseases. 
546 |a EN 
690 |a genotype 
690 |a phenotype 
690 |a next-generation sequencing 
690 |a child 
690 |a inherited liver disease 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pediatrics, Vol 9 (2021) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fped.2021.631620/full 
787 0 |n https://doaj.org/toc/2296-2360 
856 4 1 |u https://doaj.org/article/89f58b18b45d4c9bb569f061dccecfe9  |z Connect to this object online.