The oculocerebral syndrome in association with generalised hypopigmentation. A case report.
DJ Castle, T Jenkins, AA Shawinsky
S Afr Med J | Published : 1989
A 14-year-old girl with generalised hypopigmentation, mental retardation, abnormal movements, and ocular anomalies is described. It is suggested that she represents a further case of oculocerebral albinism, a rare autosomal recessive condition. Reference is made to previous similar cases.