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Up to: Syndromic disease · Neurovascular disorder · Lymphatic malformation · Microlissencephaly

Norman-Roberts syndrome

Lissencephaly syndrome, Norman-Roberts type is characterized by the association of lissencephaly type I with craniofacial anomalies (severe microcephaly, a low sloping forehead, a broad and prominent nasal bridge and widely set eyes) and postnatal growth retardation.

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This condition has no sub-types.