PRKCSH and kidney disorder: Genetic testing with a 385-gene NGS-based kidney disease panel (the Renasight test) identified heterozygous truncating pathogenic variants in <i>PKD1</i>: c.3957_3994dup p.(Asp1332Glyfs*27)) (ClinVar ID VCV003376509.1) and <i>PRKCSH</i>: c.374_375del p.(Glu125fs)) (ClinVarID VCV001048653.34).