Lissencephaly syndrome, Norman-Roberts type

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Lissencephaly syndrome, Norman-Roberts type

Synonyms: Microlissencephaly type A

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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: // Data version October 2023.

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Advocacy Organizations

National Organization for Disorders of the Corpus Callosum

The NODCC has become the leading organization for disorders of the corpus callosum seeking to raise the profile, understanding and acceptance of these disorders through education, networking, advocacy, and being a catalyst for research.

Clinical Trials

For a list of clinical trials in this disease area, please click here.