Experimental Therapeutics for Challenging Clinical Care of a Patient with an Extremely Rare Homozygous APOC2 Mutation

Figure 1

Patient’s family pedigree. The patient is originally from Sudan, and many family members live overseas. Consanguinity is present on both sides. The patient’s paternal and maternal grandparents are distantly related. The patient’s sister and one brother have similar medical history with HTG and pancreatitis, as well as DM. His maternal uncles have HTG, and his maternal grandfather was known to have had HTG.