29 November 2023
: Case report
Co-Occurring Thrombotic Thrombocytopenic Purpura and Autoimmune Hemolytic Anemia in a Child Carrying the Pathogenic SHOC2 c.4A>G (p.Ser2Gly) Variant
Rare disease
Lijun Liu1BCDE, Chanchan Hu1BFG, Zhenjie Chen1ADG*, Shuzhen Zhu2BCD, Lvchang Zhu1CEFDOI: 10.12659/AJCR.942377
Am J Case Rep 2023; 24:e942377
Figure 4. One variant in the SHOC2 gene and pedigree of the family. (A) Reference sequence; (B) proband; (C) father; and (D) mother. The family pedigree (filled black symbols represent the affected family members, and the arrows represent the proband in our research).






