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.

Also known as: Microlissencephaly type A, Norman-Roberts syndrome, lissencephaly 2, lissencephaly 2 (Norman-Roberts type), lissencephaly syndrome, Norman-Roberts type, LIS2, Norman Roberts lissencephaly syndrome, lissencephaly syndrome Norman-Roberts type

1 clinical trial for this condition and its sub-types, 0 tagged with Norman-Roberts syndrome itself.