[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$f65-g5LTUgHIk8dGZIHhGe2pKpxnfW0g-O4HGxk3yxcs":3,"$f6oQ56UBU154HD8K445-FKyyUrEIpTgN4Z1ocHd96aZw":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":41},200,"操作成功",{"id":12,"name":13,"describes":6,"symptoms":6,"checkup":6,"treatment":6,"seoTitle":14,"seoKeywords":15,"seoDescription":16,"coverVertical":6,"coverAcross":6,"introduceClassifications":17,"departments":38},2799,"先天性血管萎缩性皮肤异色症"," 先天性血管萎缩性皮肤异色症的症状和治疗方法详解"," 先天性血管萎缩性皮肤异色症, 血管萎缩性皮肤异色症, 皮肤疾病, 先天性皮肤病, 血管疾病, 皮肤异色症, 皮肤护理, 疾病治疗"," 了解先天性血管萎缩性皮肤异色症的症状、原因和治疗方法。本页面提供全面的信息，帮助您认识和管理这种罕见的皮肤疾病，提高生活质量。",[18,23,28,33],{"id":19,"classification":20,"description":21,"sort":22,"diseaseId":12},17773,"概述","\u003Cp>　　先天性血管萎缩性皮肤异色症(congenital poikiloderma atrophicans vasculare syndrome)又称Rothmund-Thomson综合征。其主症为皮肤萎缩、棕红色色素沉着、毛细血管扩张，伴有先天性白内障。\u003C/p>",0,{"id":24,"classification":25,"description":26,"sort":27,"diseaseId":12},17776,"病因","\u003Cp>　　(一)发病原因\u003C/p>\u003Cp>　　病因不明。为常染色体隐性遗传，家族中常有多个同患者，女性较男性多，上代常有近亲结婚史。其主症为皮肤萎缩、棕红色色素沉着、毛细血管扩张，伴有先天性白内障。\u003C/p>\u003Cp>　　(二)发病机制\u003C/p>\u003Cp>　　发病机制还不清楚。可能为常染色体隐性遗传。\u003C/p>",1,{"id":29,"classification":30,"description":31,"sort":32,"diseaseId":12},17779,"症状","\u003Cp>　　常见症状：凹陷瘢痕、 色素异常 、指甲异常\u003C/p>\u003Cp>　　患儿对光敏感。光照处易起大疱。3～6岁时有40%出现白内障，有些病人有角膜变性。头发、眉毛、睫毛稀少。约有25%患者出现甲生长不良，甲表面粗糙肥厚，有纵嵴。约半数患者有先天性骨发育缺陷或畸形，部分患者有生殖腺功能不全，内外生殖器发育不良，男性可有隐睾，女性无月经。\u003C/p>\u003Cp>　　根据临床表现，皮损特点的特征性即可诊断。\u003C/p>",2,{"id":34,"classification":35,"description":36,"sort":37,"diseaseId":12},17781,"检查","\u003Cp>　　检查项目：血分析\u003C/p>",3,[39,40],"眼科","皮肤科",true]