Craniosynostosis-intracranial calcification is a form of syndromic craniosynostosis, characterized by pancraniosynostosis, head circumference below the mid-parental head circumference, mild facial dysmorphism (prominent supraorbital ridges, mild proptosis and maxillary hypoplasia) and calcification of the basal ganglia. The disease is associated with a favorable neurological outcome, normal intelligence and is inherited in an autosomal recessive manner. The disease is craniosynostosis-intracranial calcifications syndrome (MONDO_0012035, a Monarch Disease Ontology term). Also known as: Longman-Tolmie syndrome.