Figure 1
From: Two new families with hereditary minimal change disease
Extensive pedigree of the first family. Three members of this Portuguese non-consanguineous family were affected by steroid-sensitive nephrotic syndrome, type minimal change disease: two affected siblings (cases 1 and 2) and the first cousin once removed (case 3). The index case (case 1) is indicated by an arrow head. The numbers inside figures indicate the number of males (square), females (rounds) or non-specified sex (lozenges) of the family.