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Fig. 1 | Experimental Hematology & Oncology

Fig. 1

From: Whole exome sequencing reveals a novel LRBA mutation and clonal hematopoiesis in a common variable immunodeficiency patient presented with hemophagocytic lymphohistiocytosis

Fig. 1

Bone marrow features: A Phagocytosis of red cells and platelets by hemophagocytichistiocytes; B Abnormal granulocytes and blast by flow cytometry; C Immunochemistry of BM specimen suggested an increase in immature myeloid cells which are positive for CD33, CD117, CD45-SSA, and CD11B; D Pedigree of the family and Sanger sequencing confirming the mutation status of LRBA in the patient and her parent, brother and son (F, father; M, mother; Patient; S, Son; B1, brother 1; B2,brother 2)

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