Title : Identification of a novel pathogenic variant in the LPL gene in lipaemia retinalis in an infant - Arya_2025_BMJ.Case.Rep_18_e259965 |
Author(s) : Arya S , Saxena S |
Ref : BMJ Case Rep , 18 : , 2025 |
Abstract :
An infant presented to the paediatric emergency department of our tertiary care centre, with failure to thrive and frequent vomiting for the past 2 days. Venous blood samples appeared pale pink. Bedside smartphone-assisted fundus examination revealed a bilateral salmon-coloured retina with creamy vasculature, suggesting lipaemia retinalis. Serum triglyceride levels of 12 100.7 mg/dL were observed. Exome sequencing confirmed the diagnosis. A novel homozygous missense variant p.Cys 291Tyr (c.872G>A) pathogenic variant in exon 6 of the lipoprotein lipase (LPL) gene was discovered. The infant was advised to undergo dietary modification and to follow-up regularly. At 1 year follow-up, the child was thriving on a low-fat diet. However, fundus examination findings persisted. |
PubMedSearch : Arya_2025_BMJ.Case.Rep_18_e259965 |
PubMedID: 40132937 |
Gene_locus related to this paper: human-LPL |
Mutation | C291Y_human-LPL |
Gene_locus | human-LPL |
Disease | Hyperlipoproteinemia TypeI |
Arya S, Saxena S (2025)
Identification of a novel pathogenic variant in the LPL gene in lipaemia retinalis in an infant
BMJ Case Rep
18 :
Arya S, Saxena S (2025)
BMJ Case Rep
18 :