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South African Medical Journal

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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.




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