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

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:C537069 (MONDO:equivalentTo)
  • SCTID:720956003 (MONDO:equivalentTo)
  • GARD:2351 (MONDO:GARD)
  • UMLS:C2931412 (MONDO:equivalentTo)
  • Orphanet:2048 (MONDO:equivalentTo)
  • MEDGEN:419406 (MONDO:equivalentTo)
Subsets

ordo_disorder, gard_rare, rare, nord_rare, orphanet_rare

exactMatch

http://identifiers.org/snomedct/720956003

http://identifiers.org/medgen/419406

http://www.orpha.net/ORDO/Orphanet_2048

http://identifiers.org/mesh/C537069

http://linkedlifedata.com/resource/umls/id/C2931412

excluded from qc check

http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql

has related synonym

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

id

MONDO:0023171

seeAlso

https://rarediseases.info.nih.gov/diseases/2351/foix-chavany-marie-syndrome