RT Journal Article SR Electronic T1 Cone and cone–rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation JF British Journal of Ophthalmology JO Br J Ophthalmol FD BMJ Publishing Group Ltd. SP 1086 OP 1091 DO 10.1136/bjo.2007.133231 VO 92 IS 8 A1 V B D Kitiratschky A1 D Nagy A1 T Zabel A1 E Zrenner A1 B Wissinger A1 S Kohl A1 H Jägle YR 2008 UL http://bjo.bmj.com/content/92/8/1086.abstract AB Aim: To describe the detailed phenotypes of a multi-generation family affected by autosomal dominant cone–rod dystrophy (adCRD) and characterised by marked intrafamilial heterogeneity, due to a novel frameshift mutation in the CRX gene.Methods: Six affected and two unaffected family members underwent detailed ophthalmological examination as well as psychophysical and electrophysiological testing. Mutation screening of the CRX gene and segregation analysis were performed in 14 family members from three generations.Results: Clinical examination of six available mutation carriers showed marked phenotypic heterogeneity, presenting with a reduced cone electroretinogram (ERG) and normal rod ERG in one family branch and a negative ERG in the other as the most striking feature. Genetic screening identified a novel mutation in the CRX gene, c.636delC, that independently segregates with the disease in both branches of the family.Conclusion: The authors identified a novel disease causing mutation in the CRX gene associated with adCRD. Furthermore, we show here for the first time the coexistence of a reduced cone and a negative ERG component in different individuals of the same family, all affected by the same mutation.