Autosomal dominant tubulointerstitial kidney disease with a novel heterozygous missense mutation in the uromodulin gene: A case report

Figure 1 Pedigree for the family of the patient, indicating individuals affected by familial hyperuricemia and chronic kidney diseases. (1) Black and gray symbols corresponding to the affected individuals, with the patient described in this case report marked with an arrow; and (2) Lines under individuals indicate people who provided DNA samples, while the two underlines denote couples with no children.