Lissencephaly syndrome, Norman-Roberts type

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Name:
Lissencephaly syndrome, Norman-Roberts type
Description:
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.
ORPHAcode:
89844
Synonyms:
Microlissencephaly type A
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14