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Normanā€“Roberts syndrome
? TBD
Medical condition
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Normanā€“Roberts syndrome is a rare form of microlissencephaly caused by a mutation in the RELN gene. A small number of cases have been described. The syndrome was first reported by Margaret Grace Norman and M. Roberts et al. in 1976.

Instance of
developmental defect during embryogenesis
Rare disease
class of disease
Subclass of
syndromic lymphedema
rare genetic immune disease
primary lymphedema with associated anomalies
genetic vascular anomaly
Microlissencephaly
Lissencephaly
Genetic disorder
autosomal recessive disease
Wikidata