Fig. 1From: Germline 3p22.1 microdeletion encompassing RPSA gene is an ultra-rare cause of isolated aspleniaLaboratory and genetic findings in the patient with isolated asplenia. A Peripheral blood smear with Howell–Jolly bodies (indicated with arrows); B Heterozygous deletion at the short arm of chromosome 3 with a size of 337.2 kbp (arr[GRCh37] 3p22.2p22.1(39357060_39694267) × 1) encompassing the RPSA gene (red arrow)Back to article page