SE-ATLAS

Craniodiaphyseal dysplasia Rare disease with Pierre Robin syndrome Isolated ankyloblepharon filiforme adnatum Non-syndromic bilambdoid and sagittal craniosynostosis Cantú syndrome Hypomandibular faciocranial dysostosis Teebi-Shaltout syndrome Maxillonasal dysplasia Oculomaxillofacial dysostosis Dysostosis with predominant craniofacial involvement Craniosynostosis Multiple pterygium-malignant hyperthermia syndrome Delayed membranous cranial ossification Isolated Pierre Robin syndrome Familial osteodysplasia, Anderson type Macroglossia Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome Treacher-Collins syndrome Hypoglossia/aglossia Isolated congenital syngnathia Simpson-Golabi-Behmel syndrome type 2 Orofacial clefting syndrome Arthrogryposis multiplex congenita-whistling face syndrome Proteus syndrome Facial cleft Van der Woude syndrome Syndrome or malformation associated with head and neck malformations Autosomal dominant popliteal pterygium syndrome Adducted thumbs-arthrogryposis syndrome, Christian type Cleidocranial dysplasia Popliteal pterygium syndrome Craniofaciofrontodigital syndrome Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome Oculoauriculovertebral spectrum with radial defects Morgagni-Stewart-Morel syndrome Monosomy 18q Simpson-Golabi-Behmel syndrome Syndrome de Goldenhar Syndrome oro-facio-digital Fente vélo-palatine Syndrome BOR Dysostose acrofaciale post-axiale Malformation crânienne Dysplasie frontonasale Syndrome de Beckwith-Wiedemann Syndrome d'ankyloblépharon-anomalies ectodermiques-fente labiopalatine Syndrome d'ankyloblépharon filiforme-imperforation anale Syndrome EEC Syndrome oto-palato-digital Syndrome de Dobrow Absence de voûte crânienne Maladie rare en chirurgie maxillo-faciale Syndrome CHARGE Dysplasie oto-mandibulaire Lacunes pariétales Syndrome de Van den Ende-Gupta Syndrome de Marden-Walker