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. [ Orphanet:2048 ]
Synonyms: foix chavany Marie syndrome
Term information
- UMLS:C2931412 (MONDO:equivalentTo)
- MEDGEN:419406 (MONDO:equivalentTo)
- MESH:C537069 (MONDO:equivalentTo)
- GARD:2351 (MONDO:GARD)
- Orphanet:2048 (MONDO:equivalentTo)
- SCTID:720956003 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, gard_rare, ordo_disorder, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__tag_existing_treatment_other, matrix_included, nord_rare, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_syndromic_disease, orphanet_rare, harrisons_view_nervous_system_disorder, mondo_top_grouping_syndromic_disease
http://identifiers.org/snomedct/720956003
http://identifiers.org/medgen/419406
http://identifiers.org/mesh/C537069
http://www.orpha.net/ORDO/Orphanet_2048
http://linkedlifedata.com/resource/umls/id/C2931412
http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
congenital Foix-Chavany-Marie syndrome (subtype)
congenital Foix-Chavany-Marie syndrome
facio-Labio-pharyngo-Glosso-laryngo-brachial paralysis
opercular syndrome, anterior
facio-pharyngo-glossal diplegia with automatic-voluntary movement dissociation
anterior opercular syndrome
facio-pharyngo-glosso-masticatory diplegia
pseudobulbar paralysis, cortical type
bilateral anterior opercular syndrome