The centre is a full member of ERN-CRANIO.
ERN-CRANIO covers rare and/or complex craniofacial anomalies and ear, nose and throat (ENT) disorders.
Full Network Expertise: Craniosynostosis; Craniofacial clefts; Encephaloceles; Fibrous Dysplasia; Neurofibromatosis; Craniofacial Microsomia; Aplasia Cutis; Facial Dysostosis; Microtia; Facial nerve palsy; Tongue anomalies; Non-syndromic cleft palate; Non-syndromic cleft lip/palate; Syndromic cleft palate; Syndromic cleft lip/palate; Robin sequence; Disorders with cleft lip/palate as important feature; Orodental anomalies as one of the presentations of at least 900 rare diseases or syndromes: Amelogenesis imperfecta; Hypodontia/oligodontia/supernumerary teeth; Dentinogenesis imperfecta/dentine dysplasia; Eruption/resorption/early loss teeth; Solitary median maxillary central incisor syndrome; Cleidocranial dysostosis; Genetic and isolated hearing loss; Laryngotracheal stenosis; Laryngotracheo-esophageal cleft; Congenital nasal anomalies; Congenital anomalies of the neck. Updated list here
The Project POST-DOC/0916/0222 is co-financed by the European Regional Development Fund and the Republic of Cyprus through the Research and Innovation Foundation. The Host Organisation is Cyprus Alliance for Rare Disorders.