APA Dictionary of Psychology

oculocerebral-hypopigmentation syndrome

Updated on 11/15/2023
a rare hereditary disorder marked by eye anomalies, absence of hair and skin pigmentation, intellectual developmental disorder, and spasticity. First identified in 1967 in three siblings of an Old Order Amish family, the syndrome is believed to be due to an autosomal recessive trait that becomes manifested through consanguinity (relationship by blood).
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