{"title":"整骨疗法操作下的组织脆性和ehers - danlos综合征整体加重","authors":"C. Hamonet","doi":"10.32474/ojnbd.2019.03.000159","DOIUrl":null,"url":null,"abstract":"Ehlers-Danlos syndrome is a hereditary, diffuse connective tissue disorder whose frequency is largely underestimated. Its diagnosis rests on a grouping of clinical criteria while biogenetic results are unreliable. Paradoxically, Ehlers-Danlos syndrome is considered as a rare disease while its prevalence in the world is at least 2%. It is very poorly known and very rarely diagnosed. This situation is dangerous for patients and exposes them to iatrogenic effects. The case reported here is a good illustration of this situation in a 26-year-old man, with local complications (paralysis of serratus major), a dramatic worsening of the disease’s symptoms (pain, proprioception) and exclusion from the work world.","PeriodicalId":93346,"journal":{"name":"Online journal of neurology and brain disorders","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Tissue Fragility and Ehlers-Danlos Syndrome Global Aggravation by Osteopathic Manipulations\",\"authors\":\"C. Hamonet\",\"doi\":\"10.32474/ojnbd.2019.03.000159\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ehlers-Danlos syndrome is a hereditary, diffuse connective tissue disorder whose frequency is largely underestimated. Its diagnosis rests on a grouping of clinical criteria while biogenetic results are unreliable. Paradoxically, Ehlers-Danlos syndrome is considered as a rare disease while its prevalence in the world is at least 2%. It is very poorly known and very rarely diagnosed. This situation is dangerous for patients and exposes them to iatrogenic effects. The case reported here is a good illustration of this situation in a 26-year-old man, with local complications (paralysis of serratus major), a dramatic worsening of the disease’s symptoms (pain, proprioception) and exclusion from the work world.\",\"PeriodicalId\":93346,\"journal\":{\"name\":\"Online journal of neurology and brain disorders\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-10-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Online journal of neurology and brain disorders\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32474/ojnbd.2019.03.000159\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Online journal of neurology and brain disorders","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32474/ojnbd.2019.03.000159","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Tissue Fragility and Ehlers-Danlos Syndrome Global Aggravation by Osteopathic Manipulations
Ehlers-Danlos syndrome is a hereditary, diffuse connective tissue disorder whose frequency is largely underestimated. Its diagnosis rests on a grouping of clinical criteria while biogenetic results are unreliable. Paradoxically, Ehlers-Danlos syndrome is considered as a rare disease while its prevalence in the world is at least 2%. It is very poorly known and very rarely diagnosed. This situation is dangerous for patients and exposes them to iatrogenic effects. The case reported here is a good illustration of this situation in a 26-year-old man, with local complications (paralysis of serratus major), a dramatic worsening of the disease’s symptoms (pain, proprioception) and exclusion from the work world.