The oculocerebral syndrome in association with generalised hypopigmentation A case report

  • DJ Castle
  • T Jenkins
  • A. A. Shawinsky

Abstract

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.

Section
Articles

Journal Identifiers


eISSN: 0256-95749
print ISSN: 2078-5135