Wilson disease associated with immune thrombocytopenia: A case report and review of the literature

Figure 1 Wilson disease patient’s family pedigree showing the mutations detected in ATP7B. A: The family pedigree. The arrow indicates the proband; her parents had no signs of Wilson disease; B: Non-synonymous mutations detected in the family. The proband had both mutations, while the c.3809A>G mutation was only detected in her mother and the c.2333G>T mutation was only detected in her father.