{"orpha":206991,"name":"Viral myositis","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":[],"definition":"A rare acquired skeletal muscle disease characterized by sudden onset of muscle weakness, tenderness, and pain during or following recovery from a viral illness. The most commonly reported underlying viral infections are influenza B and A, the latter being the significantly less frequent cause. Most cases occur in children. Symptoms are often limited to the calf muscles, but other muscle groups may be involved as well. The condition is typically self-limiting, resolving within several days, although rhabdomyolysis with renal failure and compartment syndrome have been reported.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-206991/","orphanet_url":"https://www.orpha.net/en/disease/detail/206991","names":{"fr":{"name":"Myosite virale","definition":"Maladie musculaire squelettique acquise rare caractérisée par l'apparition soudaine d'une faiblesse, d'une sensibilité et d'une douleur musculaires pendant ou après la rémission à la suite d'une maladie virale. Les infections virales sous-jacentes les plus fréquemment rapportées sont les grippes B et A, cette dernière étant la cause la moins fréquente. La plupart des cas se produisent chez les enfants. Les signes cliniques sont souvent limités aux muscles du mollet, mais d'autres groupes de muscles peuvent également être affectés. La maladie se résorbe spontanément et disparaît en quelques jours, bien qu'une rhabdomyolyse avec insuffisance rénale et un syndrome des loges aient été rapportés."},"de":{"name":"Myositis, virale","definition":"Eine seltene erworbene Skelettmuskelerkrankung, die durch plötzliches Auftreten von Muskelschwäche, Empfindlichkeit und Schmerzen während oder nach der Genesung von einer Viruserkrankung gekennzeichnet ist. Die am häufigsten gemeldeten zugrunde liegenden Virusinfektionen sind Influenza B und A, wobei letztere die deutlich seltenere Ursache ist. Die meisten Fälle treten bei Kindern auf. Die Symptome beschränken sich häufig auf die Wadenmuskeln, es können aber auch andere Muskelgruppen betroffen sein. Die Erkrankung ist in der Regel selbstlimitierend und klingt innerhalb weniger Tage ab, obwohl auch über Rhabdomyolyse mit Nierenversagen und Kompartmentsyndrom berichtet wurde."},"es":{"name":"Miositis viral","definition":"Es una enfermedad adquirida y poco frecuente del músculo esquelético caracterizada por la aparición repentina de debilidad muscular, sensibilidad y dolor durante o después del periodo de recuperación de una enfermedad viral. Las infecciones virales subyacentes descritas con más frecuencia son la influenza B y A, siendo esta última mucho menos frecuente. La mayoría de los casos ocurren en niños. Los síntomas a menudo se limitan a los músculos de la pantorrilla, pudiendo afectar también a otros grupos musculares. Por lo general, la afección es autolimitada y remite en varios días, aunque se ha descrito rabdomiólisis con insuficiencia renal y síndrome compartimental."},"it":{"name":"Miosite virale","definition":"Si tratta di una malattia muscoloscheletrica acquisita rara, caratterizzata da debolezza muscolare ad esordio improvviso, sensibilità e dolore durante o dopo la guarigione di una malattia virale, più comunemente l'influenza B e A (quest'ultima è significativamente meno frequente). La malattia colpisce per lo più i bambini. I sintomi in genere sono limitati ai muscoli del polpaccio, ma possono interessare anche altri gruppi muscolari. Di solito la malattia è autolimitante e si risolve nell'arco di qualche giorno, ma sono stati descritti casi di rabdomiolisi con insufficienza renale e sindrome compartimentale."},"nl":{"name":"Virale myositis","definition":"Een zeldzame, verworven aandoening van skeletspier, gekarakteriseerd door plotse aanvang van zwakte, gevoeligheid en pijn van spieren tijdens of na een virale ziekte. De meest gerapporteerde onderliggende virale infecties zijn influenza B en A, waarvan deze laatste significant minder frequent voorkomt als oorzaak. De meeste gevallen komen voor bij kinderen. Symptomen blijven vaak beperkt tot kuitspieren, maar andere spiergroepen kunnen eveneens betrokken zijn. De aandoening is doorgaans zelfbeperkend en verdwijnt binnen enkele dagen, hoewel reeds rabdomyolyse met nierfalen en compartimentsyndroom werden gerapporteerd."},"pt":{"name":"Miosite viral"},"pl":{"name":"Wirusowe zapalenie mięśni"},"cs":{"name":"Virová myozitida"},"uk":{"name":"Вірусний міозит","definition":"A rare acquired skeletal muscle disease characterized by sudden onset of muscle weakness, tenderness, and pain during or following recovery from a viral illness. The most commonly reported underlying viral infections are influenza B and A, the latter being the significantly less frequent cause. Most cases occur in children. Symptoms are often limited to the calf muscles, but other muscle groups may be involved as well. The condition is typically self-limiting, resolving within several days, although rhabdomyolysis with renal failure and compartment syndrome have been reported."},"zh":{"name":"病毒性肌炎","definition":"病毒性肌炎是一种罕见的获得性骨骼肌疾病，其主要临床表现为病毒感染性疾病恢复期或之后突然出现肌无力、肌肉压痛和疼痛，乙型流感病毒和甲型流感病毒最常见，前者更常见，常发生于儿童期。症状往往局限于小腿肌肉，但也可累及其他肌肉群，该病为自限性疾病，能在几天内好转，但部分患者会出现横纹肌溶解症伴肾功能不全和室间隔综合征。"},"tr":{"name":"Viral miyozit"}},"xrefs":[{"source":"ICD-10","code":"M60.0","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"FB30","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"864399177"},{"source":"MONDO","code":"0016126","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0150005","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10051512","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68416,"name":"Rare infectious disease"},"parents":[{"orpha":206988,"name":"Infectious, fungal or parasitic myopathy","classifications":[181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["All ages"],"prevalence":[],"phenotypes":null}