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720956003: Foix Chavany Marie syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3322637018 Foix Chavany Marie syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3322638011 Foix Chavany Marie syndrome en Synonym Active Case sensitive SNOMED CT core
3322639015 Bilateral anterior opercular syndrome en Synonym Active Case insensitive SNOMED CT core
3322640018 Facio-pharyngo-glosso-masticatory diplegia en Synonym Active Case insensitive SNOMED CT core
3322641019 Acortico-subcortical suprabulbar or pseudobulbar palsy of the lower cranial nerves, with characteristics of 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. Less than 150 cases have been described in the literature so far. Can occur at any age. Patients have severe speech disturbances and most are mute.Chewing and swallowing are severely impaired. Caused by developmental or acquired bilateral lesions of the anterior opercula. In children, it presents congenitally (bilateral opercular polymicrogyria) or as an acquired disorder due to encephalitis, epilepsy and neurodegenerative disorders. The syndrome is generally sporadic but some familial cases have been described. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Foix Chavany Marie syndrome Is a Multiple cranial nerve palsy true Inferred relationship Some
Foix Chavany Marie syndrome Finding site Cranial nerve structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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