Furthermore, three patients had variants linked to familial chylomicronemia syndrome: one was compound heterozygous for two likely pathogenic variants in LPL, another was homozygous for a likely pathogenic variant in LMF1, and the third was heterozygous for a likely pathogenic variant in LPL (Table 1). The gene discussed is LMF1; the disease is familial chylomicronemia syndrome.