Lissencephaly syndrome, Norman-Roberts type

Orpha code: 89844OMIM code: 257320

Definition

Lissencephaly syndrome, Norman-Roberts type is characterised 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.

Disease data
Classification

Clinical subtype

Synonyms
Microlissencephaly type A
Mikrolizencefalia typu A
ORPHA code
89844
OMIM code
257320
ICD10 code
Q04.3
ICD11 code
-

No additional description.

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