{"orpha":2809,"name":"Familial recurrent peripheral facial palsy","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":["Familial recurrent Bell palsy"],"definition":"A rare peripheral neuropathy characterized by an acute onset of unilateral facial muscle weakness with Bell's phenomenon. It is non-progressive, resolves spontaneously, and it might be recurrent with no obvious precipitating factors.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-2809/","orphanet_url":"https://www.orpha.net/en/disease/detail/2809","names":{"fr":{"name":"Paralysie faciale périphérique récurrente familiale","synonyms":["Paralysie de Bell récurrente familiale"],"definition":"Neuropathie périphérique rare caractérisée par l'apparition soudaine d'une faiblesse unilatérale des muscles faciaux accompagnée du signe de Bell. Non progressive et spontanément résolutive, la maladie peut toutefois récidiver sans qu'aucun facteur précipitant ne soit connu."},"de":{"name":"Fazialisparese, periphere rekurrente, familiäre Form","synonyms":["Gesichtslähmung, familiäre rekurrente"]},"es":{"name":"Parálisis facial periférica familiar recurrente","synonyms":["Parálisis familiar recurrente de Bell"],"definition":"La parálisis facial periférica familiar recurrente es una neuropatía periférica poco frecuente, caracterizada por un inicio agudo de debilidad muscular facial unilateral con fenómeno de Bell. No es progresiva, se resuelve espontáneamente y puede recurrir en ausencia de factores desencadenantes conocidos."},"it":{"name":"Paralisi facciale periferica ricorrente familiare","definition":"La paralisi facciale periferica ricorrente familiare è una neuropatia periferica rara, caratterizzata da debolezza monolaterale dei muscoli facciali ad esordio acuto con fenomeno di Bell. La malattia non è progressiva, si risolve spontaneamente e può recidivare anche in assenza di evidenti fattori scatenanti."},"nl":{"name":"Familiale recurrente perifere facialisparalyse","synonyms":["Familiale recurrente perifere aangezichtsverlamming van Bell"],"definition":"Familiale recurrente perifere facialisparalyse is een zeldzame perifere neuropathie die gekarakteriseerd wordt door een acute aanvang van unilaterale zwakte van gelaatsspieren met fenomeen van Bell. Het is niet-progressief, verdwijnt spontaan, en kan terugkeren zonder duidelijke precipiterende factoren."},"pt":{"name":"Paralisia facial periférica recorrente familiar","synonyms":["Paralisia familiar recorrente de Bell"]},"pl":{"name":"Rodzinne nawracające obwodowe porażenie twarzy","synonyms":["Rodzinne nawracające porażenie twarzy Bella"],"definition":"*Rodzinne nawracające obwodowe porażenie twarzy jest rzadką neuropatią obwodową, która charakteryzuje się jednostronnym osłabieniem mięśni twarzy o wczesnym początku, z towarzyszącym objawem Bella. Choroba nie postępuje, ustępuje samoistnie i może nawracać bez wyraźnych czynników wywołujących."},"cs":{"name":"Familiární rekurentní periferní obrna","synonyms":["Familial recurrent Bell palsy"]},"uk":{"name":"Сімейний рецидивуючий периферичний параліч обличчя","synonyms":["Сімейний рецидивуючий параліч Белла"],"definition":"A rare peripheral neuropathy characterized by an acute onset of unilateral facial muscle weakness with Bell's phenomenon. It is non-progressive, resolves spontaneously, and it might be recurrent with no obvious precipitating factors."},"zh":{"name":"家族性复发性外周性面瘫","synonyms":["家族性复发性贝尔麻痹"]},"tr":{"name":"Ailesel tekrarlayan periferik yüz felci","synonyms":["Ailesel tekrarlayan Bell felci"]}},"xrefs":[{"source":"OMIM","code":"134200","qualifier":"E","icd_relation":null,"validated":true},{"source":"ICD-10","code":"G51.0","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"8B88.0","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"MONDO","code":"0007592","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C565028","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1851399","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":98497,"name":"Genetic peripheral neuropathy","classifications":[156,181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["Adolescent","Adult","Childhood"],"prevalence":[{"type":"Annual incidence","qualification":"Value and class","class":"1-9 / 100 000","value":5.6,"area":"Worldwide","status":"Validated","source":"38435234[PMID]_ORPHANET"}],"phenotypes":null}