Nicu C, Damian C, Glavici M
Secţia Oftalmologie, Drobeta-Turnu-Severin.
Oftalmologia. 1993 Jul-Sep;37(3):256-60.
The paper presents the case of an 11 years-old child with secondary pigmentary retinopathy, atrial septal defect, facial dysmorphia with mandibular hypoplasia: all these malformations are part of the congenital rubeola syndrome. The patient has a twin brother presenting similar manifestations, but having a different expressivity.