The oculocerebral syndrome in association with generalised hypopigmentation. A case report
Castle, D.J.; Jenkins, T.; Shawinsky, A.A.
South African Medical Journal 76(1): 35-36
1989
ISSN/ISBN: 0256-9574 PMID: 2500717 Document Number: 346837
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.
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