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Norman-Roberts syndrome
rareLissencephaly 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.
- Identifiers
- MONDO:0009760 OMIM:257320Orphanet:89844
- 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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