OCULOCEREBRAL-HYPOPIGMENTATION SYNDROME

a genetic disorder characterized by eye anomalies, lack of hair and skin pigmentation, cognitive impairment, and spasticity. The cases examined have comprised kids of Old Order Amish families. The syndrome is thought to be a consequence of an autosomal recessive trait which becomes created by way of consanguinity.

OCULOCEREBRAL-HYPOPIGMENTATION SYNDROME: “Oculocerebral-hypopigmentation syndrome is not a diagnosis to be taken lightly.”

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PLEASURE PRINCIPLE

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