Familial episodic pain syndrome (original) (raw)

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dbo:abstract Familial episodic pain syndrome, also known simply as FEPS, is a group of rare genetic peripheral neuropathies which are characterized by recurrent random episodes of intense pain which occur most often in the upper or lower parts of the body occurring in several members of the same family. They are often triggered by cold temperatures, physical exercise, fatigue, etc. It may or may not get better with age. (en)
dbo:alias (en) FEPS (en)
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dbo:wikiPageWikiLink dbc:Chronic_pain_syndromes dbc:Rare_genetic_syndromes dbr:Colombia dbr:Genetic_mutation dbr:Analgesics dbr:Fatigue dbr:Pain dbr:Physical_exercise dbr:Medical_genetics dbr:Chromosome_3 dbr:Chromosome_8 dbr:China dbr:Cold dbr:Neurology dbr:SCN10A dbr:TRPA1 dbr:SCN11A dbr:Peripheral_neuropathies
dbp:causes Autosomal dominant genetic mutation (en)
dbp:complications Walking impairment. (en)
dbp:deaths - (en)
dbp:frequency very rare, around 16 families have been described in medical literature. (en)
dbp:name Familial episodic pain syndrome (en)
dbp:onset Depends on the type (en)
dbp:prevention None (en)
dbp:prognosis Medium (en)
dbp:specialty dbr:Medical_genetics dbr:Neurology
dbp:symptoms Intense episodic pain occurring within people of the same families. (en)
dbp:synonyms FEPS (en)
dbp:treatment Analgesics, anti-inflammatory medication. (en)
dbp:types FEPS type 1, 2 and 3. (en)
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dcterms:subject dbc:Chronic_pain_syndromes dbc:Rare_genetic_syndromes
rdf:type owl:Thing wikidata:Q12136 dbo:Disease
rdfs:comment Familial episodic pain syndrome, also known simply as FEPS, is a group of rare genetic peripheral neuropathies which are characterized by recurrent random episodes of intense pain which occur most often in the upper or lower parts of the body occurring in several members of the same family. They are often triggered by cold temperatures, physical exercise, fatigue, etc. It may or may not get better with age. (en)
rdfs:label Familial episodic pain syndrome (en)
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