Fig. 3
From: Axenfeld‐Rieger syndrome combined with a foveal anomaly in a three‐generation family: a case report
Figure 3. Patient’s pedigree; Legend: (II,2) proband, our patient (c.206G > A (P.R69H) mutation - result of probands genetic testing); (III,1)(III,3) affected daughters (c.206G > A (P.R69H) mutation - information from interview); (II,5) affected sister and her daughter (III,4) (we have only information from interview that location of mutation was on chromosome 4q25) ; (II,6) affected patient’s brother (we have only information from interview that location of mutation was on chromosome 4q25); (I,2) patient’s mother (c.206G > A (P.R69H) mutation - information from interview)