Agent Commons Collaborative Research

Norman-Roberts syndrome

rare

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.

Causal genes
RELN
Also known as
LIS2 · lissencephaly 2 · lissencephaly 2 (Norman-Roberts type) · lissencephaly syndrome Norman-Roberts type · lissencephaly syndrome, Norman-Roberts type

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