Clinical feature and molecular diagnostic analysis of the first non-caucasian child with infantile liver failure syndrome type 1.
- Author:
Wei-Xia LIN
1
;
Qi-Qi ZHENG
;
Li GUO
;
Ying CHENG
;
Yuan-Zong SONG
Author Information
1. Department of Pediatrics, First Affiliated Hospital, Jinan University, Guangzhou 510630, China. songyuanzong@hotmail.com.
- Publication Type:Case Reports
- MeSH:
Child, Preschool;
High-Throughput Nucleotide Sequencing;
Humans;
Leucine-tRNA Ligase;
genetics;
Liver Failure;
diagnosis;
genetics;
Male;
Mitochondrial Membrane Transport Proteins;
genetics;
Mutation
- From:
Chinese Journal of Contemporary Pediatrics
2017;19(8):913-920
- CountryChina
- Language:Chinese
-
Abstract:
Infantile liver failure syndrome type 1 (ILFS1) is a Mendelian disease due to biallelic mutations in the cytoplasmic leucyl-tRNA synthetase gene (LARS). This study aimed to report the clinical and molecular features of the first non-caucasian ILFS1 patient, providing reliable evidences for the definite diagnosis of ILFS1. The 2 years and 9 months old male patient was referred to the hospital with hepatosplenomegaly over 1 year. At age 17 months, he was found to have hepatosplenomegaly and anemia. Since then, he had been managed in different hospitals. The laboratory tests showed liver dysfunction, hypoproteinemia, coagulopathy and anemia, along with histologically-confirmed cirrhosis and fatty liver; however, the etiology remained undetermined. The subsequent SLC25A13 mutation analysis by means of prevalent mutation screening and Sanger sequencing only revealed a paternally-inherited mutation c.1658G>A, and no aberrant SLC25A13 transcripts could be detected from the maternal allele on cDNA cloning analysis, ruling out the possibility of citrin deficiency. Further target exome high-throughout sequencing of genes relevant to genetic liver diseases detected a paternal c.2133_2135del (p.L712del) and a maternal c.1183G>A (p.D395N) mutation in LARS gene. This finding was then confirmed by Sanger sequencing, and ILFS1 was thus definitely diagnosed. The child has been followed up till age 4 years, and his condition became stabilized.
