Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report

Figure 1 Comparison of the different variation at the c. 613G>C (p.V205L) in the LHX3 gene. A: Novel variant in c.613G>C (p.V205L) of the LHX3 gene in this patient; B: No variant in the patient’s father; C: Same variant in the patient’s mother; D: Same variant in the patient’s older brother.

Figure 2 Comparison of the different variation at the c. 220T>C (p.C74R) in the LHX3 gene. A: Novel variant in c.220T>C (p.C74R) of the LHX3 gene in this patient; B: Same variant in the patient’s father; C: No variant in the patient’s mother; D: Same variant in the patient’s older brother.