Fig. 3From: Lowe syndrome identified in the offspring of an oocyte donor who was an unknown carrier of a de novo mutation: a case report and review of the literatureA hereditary pedigree showing the affected members of the family. Donor (carrier of a de novo OCRL mutation) and her daughter (also carrier). No other family member (even her two brothers) is affected by Lowe syndrome or carries the mutation causing Lowe syndrome or Dent diseaseBack to article page