disease has feature multiple cranial nerve palsy facial paralysis syndromic disease foix chavany Marie syndrome https://rarediseases.info.nih.gov/diseases/2351/foix-chavany-marie-syndrome https://www.malacards.org/card/foix_chavany_marie_syndrome MONDO:0023171 MEDGEN:419406 congenital Foix-Chavany-Marie syndrome (subtype) MESH:C537069 Orphanet:2048 Foix-Chavany-Marie syndrome (FCMS) is a cortico-subcortical suprabulbar or pseudobulbar palsy of the lower cranial nerves, characterized by severe dysarthria and dysphagia associated with bilateral central facio-pharyngo-glosso-masticatory paralysis, with prominent automatic-voluntary dissociation in which involuntary movements of the affected muscles are preserved. congenital Foix-Chavany-Marie syndrome bilateral anterior opercular syndrome opercular syndrome, anterior UMLS:C2931412 SCTID:720956003 anterior opercular syndrome pseudobulbar paralysis, cortical type facio-Labio-pharyngo-Glosso-laryngo-brachial paralysis foix chavany Marie syndrome facio-pharyngo-glossal diplegia with automatic-voluntary movement dissociation GARD:0002351