[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$f65-g5LTUgHIk8dGZIHhGe2pKpxnfW0g-O4HGxk3yxcs":3,"$fCMrYqDTPeyjBr86DeMXCaV72umenNOaymTnyA4kDUtc":8},{"code":4,"msg":5,"message":6,"data":6,"success":7},401,"认证失败，无法访问系统资源",null,false,{"code":9,"msg":10,"message":6,"data":11,"success":37},200,"操作成功",{"id":12,"name":13,"describes":6,"symptoms":6,"checkup":6,"treatment":6,"seoTitle":6,"seoKeywords":6,"seoDescription":6,"coverVertical":6,"coverAcross":6,"introduceClassifications":14,"departments":35},8118,"外耳道闭锁",[15,20,25,30],{"id":16,"classification":17,"description":18,"sort":19,"diseaseId":12},127566,"概述","\u003Cp>　　先天性小耳及外耳道闭锁常合并发生，系胚胎发育过程中第一，第二鳃弓或第一鳃沟发育不全所致，可伴有第一咽囊发育不全所引起的咽鼓管、鼓室或乳突畸形。\u003C/p>",0,{"id":21,"classification":22,"description":23,"sort":24,"diseaseId":12},127567,"症状","\u003Cp>　　常见症状：听力减退、头痛、耳朵朦胧感\u003C/p>\u003Cp>　　分型：第一型：耳廓较正常为小，外耳道及鼓膜存在，适应听力尚可。第二型：耳廓畸形，外耳遭闭锁，鼓膜及锤骨柄未发育，砧骨体与锤骨小头融合，镫骨巳育或未育。呈传音性聋，此型多见。第三型：耳廓畸形较重，外耳遭闭锁，听骨畸形，合并非鳃源性内耳畸形。内耳功能丧失。第二型、第三型有时伴有颌面发育不全，称Treacher-Collins氏综合症。颞骨CT：外耳遭闭锁，鼓室狭小，听骨畸形。\u003C/p>",1,{"id":26,"classification":27,"description":28,"sort":29,"diseaseId":12},127568,"检查","\u003Cp>　　检查项目：外耳道检查、听力检查\u003C/p>",2,{"id":31,"classification":32,"description":33,"sort":34,"diseaseId":12},127569,"治疗","\u003Cp>　　治疗原则 手术切除瘢痕松解挛缩，恢复外耳道形态口径大小及其传导功能。用肉面朝外的中厚皮片包裹橡皮或塑料管植入。皮片成活后继续支撑6个月防止回缩。外耳道口的膜状瘢痕或蹼状瘢痕可用局部交错皮瓣或行“Z”成形术修复。\u003C/p>",3,[36],"整形外科",true]