Severe course with lethal hepatocellular injury and skeletal muscular dysgenesis in a neonate with infantile liver failure syndrome type 1 caused by novel LARS1 mutations.
Katsuya HirataNobuhiko OkamotoChihiro IchikawaShouta InoueMasatoshi NozakiKimihiko BannoToshiki TakenouchiHisato SuzukiKenjiro KosakiPublished in: American journal of medical genetics. Part A (2020)
Infantile liver failure syndrome type 1 (ILFS1) is a recently recognized autosomal recessive disorder caused by deleterious mutations in the leucyl-tRNA synthetase 1 gene (LARS1). The LARS1 enzyme is responsible for incorporation of the amino acid leucine during protein polypeptide synthesis. Individuals with LARS1 mutations typically show liver failure from infancy to early childhood during periods of illness or other physiological stress. While 25 patients from 15 families with ILFS1 have been reported in the literature, histological reports from autopsy findings are limited. We report here a premature male neonate who presented with severe intrauterine growth retardation, microcytic anemia, and fulminant liver failure, and who was a compound heterozygote for two novel deleterious mutations in LARS1. An autopsy showed fulminant hepatitis-like hepatocellular injury and fibrogenesis in the liver and a lack of uniformity in skeletal muscle, accompanied by the disruption of striated muscle fibers. Striking dysgenesis in skeletal muscle detected in the present case indicates the effect of LARS1 functional deficiency on the musculature. Whole-exome sequencing may be useful for neonates with unexplained early liver failure if extensive genetic and metabolic testing is inconclusive.
Keyphrases
- liver failure
- skeletal muscle
- hepatitis b virus
- amino acid
- end stage renal disease
- insulin resistance
- chronic kidney disease
- systematic review
- ejection fraction
- early onset
- copy number
- type diabetes
- case report
- intellectual disability
- adipose tissue
- body composition
- metabolic syndrome
- preterm infants
- drug induced
- stress induced
- weight loss
- autism spectrum disorder
- weight gain
- adverse drug
- muscular dystrophy
- patient reported
- iron deficiency
- preterm birth