产前诊断遗传检测怎么选？渭南市妇幼保健院为你揭秘生命起点的“守护密码”
<div class="wx_rich_media_content" id="jsWxContainer"><section data-role="outer" label="edit by 135editor" data-pm-slice="0 0 []"><section data-tools="135编辑器" data-id="165702"><section style="margin: 10px auto;"><section style="width: 100%;height: 1px;border-top: 1px solid #6daaff;max-width:100% !important;box-sizing:border-box;" data-width="100%"><span leaf=""><br></span></section><section style="border-left: 1px solid #6daaff;border-right: 1px solid #6daaff;padding: 13px 6px;margin: -8px 6px;box-sizing:border-box;"><section style="background-color: #f1f7ff;border-radius: 10px;padding: 10px;box-sizing:border-box;"><section data-autoskip="1" style="text-align: justify; line-height: 1.75em; letter-spacing: 1.5px; color: rgb(51, 51, 51); background-color: transparent;"><p><strong><span style="text-decoration-style: solid; text-decoration-color: rgb(51, 51, 51); font-family: mp-quote, -apple-system-font, BlinkMacSystemFont, Arial, sans-serif;"><span leaf="">近日，渭南市妇幼保健院产前诊断技术正式获准开展，填补了我市产前诊断领域的专业空白，为万千孕产妇筑起更坚实的出生缺陷防控防线。为帮助准爸妈们科学认知遗传相关知识，从容应对孕期检查，我院医学遗传科将推出系列科普内容，带您读懂这项守护宝宝健康的“超前”技术。</span></span></strong></p></section></section></section><section style="width: 100%;height: 1px;border-bottom: 1px solid #6daaff;max-width:100% !important;box-sizing:border-box;" data-width="100%"><span leaf=""><br></span></section></section></section></section><section data-role="outer" label="Powered by 135editor.com onekey" style="font-size:16px;font-family:Optima-Regular,PingFangTC-Light,微软雅黑;" data-pm-slice="0 0 []"><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><span textstyle="" style="font-size: 16px;">每一对准父母心中，都藏着对健康宝宝的热切期盼。随着医学技术的飞速发展，产前遗传学检测已成为守护生命起点的重要“武器”，它就像一扇提前洞察胎儿遗传健康的窗口，帮家庭和医生排查潜在风险，为后续医疗决策与家庭规划提供科学依据。今天，渭南市妇幼保健院就带大家读懂这些“高科技检测手段”，告别选择困惑。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><section><section style="margin: 10px auto;display: flex;justify-content: center;"><section style="background: linear-gradient(to right,#d1f4ea,#ffffff);padding: 5px;box-sizing:border-box;"><section style="background-color: #6eb4f5;padding: 4px 15px;box-sizing:border-box;"><section style="color: rgb(255, 255, 255); text-align: center;"><strong data-brushtype="text"><span leaf=""><span textstyle="">一、常见产前诊断遗传检测技术详解</span></span></strong></section></section></section></section></section><section data-page-id="XJ2Gf1uIQd8SQDcyke4cH9qqnBd" data-lark-html-role="root" data-docx-has-block-data="false"><h3 style="font-size: 17px;"><span leaf=""><br></span></h3><section data-role="title" data-tools="135编辑器" data-id="165405"><section style="margin: 10px auto;display: flex;justify-content: flex-start;align-items: center;"><section style="flex-shrink: 0;"><section style="color: rgb(255, 255, 255); text-align: center; background: linear-gradient(rgb(250, 147, 82), rgb(255, 255, 255)); padding: 4px 7px; box-sizing: border-box;"><strong><span leaf=""><span textstyle="">0</span></span></strong><strong data-original-title="" title="" data-num="3"><span leaf=""><span textstyle="">1</span></span></strong></section></section><section><section style="color: rgb(23, 108, 195); padding-right: 10px; padding-left: 10px; box-sizing: border-box;"><strong data-brushtype="text"><span leaf=""><span textstyle="">胎儿染色体核型分析——经典基础的“染色体全家福”</span></span></strong></section></section></section></section></section><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="text-indent: 2.21428em;caret-color: red;"><span leaf=""><span textstyle="" style="font-size: 16px;">这项技术就像给胎儿的23对染色体拍一张完整“全家福”，医生通过显微镜观察染色体的数目和宏观结构，判断是否存在染色体数量异常（如多一条、少一条），或是大片段的缺失、重复、断裂、错误连接等结构问题。作为产前遗传诊断的“金标准”之一，它是最经典、最基础的核心检测技术。</span></span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">局限性：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">检测分辨率有限，仅能发现5-10Mb以上的明显异常，且需要进行细胞培养，报告周期相对较长，约3-4周。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><section data-tools="135编辑器" data-id="165405"><section style="margin: 10px auto;display: flex;justify-content: flex-start;align-items: center;"><section style="flex-shrink: 0;"><section style="color: rgb(255, 255, 255); text-align: center; background: linear-gradient(rgb(250, 147, 82), rgb(255, 255, 255)); padding: 4px 7px; box-sizing: border-box;"><strong><span leaf=""><span textstyle="">0</span></span></strong><strong><span leaf=""><span textstyle="">2</span></span></strong></section></section><section><section style="color: rgb(23, 108, 195); padding-right: 10px; padding-left: 10px; box-sizing: border-box;"><strong data-brushtype="text"><span leaf=""><span textstyle=""> 荧光原位杂交（FISH）——快速解忧的“靶向检查”</span></span></strong></section></section></section></section><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><span textstyle="" style="font-size: 16px;">该技术主打“快速精准”，专门针对21、18、13号染色体及性染色体（X、Y）进行检测，可快速判断这五条染色体的数目是否正常，同时辅助鉴别部分难以确定的染色体重排问题。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">优势：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">无需细胞培养，24-48小时就能出结果，能快速明确胎儿是否患有唐氏综合征（21三体）、爱德华氏综合征（18三体）等常见染色体疾病，有效缓解孕妇等待期间的焦虑情绪。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">局限性：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">检测范围较窄，仅能针对预设的特定染色体，无法排查其他染色体的异常。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><section style="text-align: center;" nodeleaf=""><span class="wxart_image" wx-style="display:inline-block;"></span></section><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><section data-tools="135编辑器" data-id="165405"><section style="margin: 10px auto;display: flex;justify-content: flex-start;align-items: center;"><section style="flex-shrink: 0;"><section style="color: rgb(255, 255, 255); text-align: center; background: linear-gradient(rgb(250, 147, 82), rgb(255, 255, 255)); padding: 4px 7px; box-sizing: border-box;"><strong><span leaf=""><span textstyle="">03</span></span></strong></section></section><section><section style="color: rgb(23, 108, 195); padding-right: 10px; padding-left: 10px; box-sizing: border-box;"><strong data-brushtype="text"><span leaf=""><span textstyle="">染色体微阵列分析（CMA）——高精度的“染色体扫描仪”</span></span></strong></section></section></section></section><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><span textstyle="" style="font-size: 16px;">如果说核型分析是“拍全家福”，CMA就像是用高精度扫描仪逐段检查染色体，能检测出全染色体非整倍体、微小片段缺失/重复综合征，以及杂合性缺失（LOH）等细微异常，分辨率比核型分析高出上千倍，可发现几十到几百kb的微小病变。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">优势：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">已成为胎儿超声结构异常、智力障碍等情况的一线诊断技术，无需细胞培养，报告周期1-2周，能精准捕捉核型分析无法发现的“隐性异常”，在超声异常但核型分析正常的胎儿中，可额外提升6%的诊断率。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">局限性：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">检测成本较高，芯片探针覆盖范围有限，无法检出染色体平衡易位、罗氏易位等平衡性结构重排。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><section data-tools="135编辑器" data-id="165405"><section style="margin: 10px auto;display: flex;justify-content: flex-start;align-items: center;"><section style="flex-shrink: 0;"><section style="color: rgb(255, 255, 255); text-align: center; background: linear-gradient(rgb(250, 147, 82), rgb(255, 255, 255)); padding: 4px 7px; box-sizing: border-box;"><strong><span leaf=""><span textstyle="">0</span></span></strong><strong data-num="3"><span leaf=""><span textstyle="">4</span></span></strong></section></section><section><section style="color: rgb(23, 108, 195); padding-right: 10px; padding-left: 10px; box-sizing: border-box;"><strong data-brushtype="text"><span leaf=""><span textstyle="">低深度全基因组测序（CNV-Seq）——高性价比的“精准替代方案”</span></span></strong></section></section></section></section><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><span textstyle="" style="font-size: 16px;">这项技术与CMA检测效能高度重叠，同样可排查全染色体非整倍体、染色体微缺失/重复综合征，核心优势在于“性价比更高”。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">优势：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">无需细胞培养，测序通量高，报告周期1-2周，成本低于CMA，适合作为广泛筛查的优选方案之一。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">局限性：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">无法检测三倍体、多倍体、杂合性缺失（LOH），以及染色体平衡性结构重排。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><section data-tools="135编辑器" data-id="165405"><section style="margin: 10px auto;display: flex;justify-content: flex-start;align-items: center;"><section style="flex-shrink: 0;"><section style="color: rgb(255, 255, 255); text-align: center; background: linear-gradient(rgb(250, 147, 82), rgb(255, 255, 255)); padding: 4px 7px; box-sizing: border-box;"><strong><span leaf=""><span textstyle="">0</span></span></strong><strong data-num="4"><span leaf=""><span textstyle="">5</span></span></strong></section></section><section><section style="color: rgb(23, 108, 195); padding-right: 10px; padding-left: 10px; box-sizing: border-box;"><strong data-brushtype="text"><span leaf=""><span textstyle="">全外显子组测序（WES）——疑难病例的“基因解码仪”</span></span></strong></section></section></section></section><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><span textstyle="" style="font-size: 16px;">外显子是基因中负责编码蛋白质的核心区域，WES技术聚焦这一关键部位，逐行排查基因“核心代码”中的变异，精准寻找导致疾病的单基因变异。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">应用场景：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">主要用于超声提示胎儿结构异常，但核型分析、CMA/CNV-Seq检测结果均正常的疑难病例，为这类家庭进一步明确病因提供重要依据。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><section data-tools="135编辑器" data-id="156959"><section style="margin: 10px auto;display: flex;justify-content: center;"><section style="background: linear-gradient(to right,#d1f4ea,#ffffff);padding: 5px;box-sizing:border-box;"><section style="background-color: #6eb4f5;padding: 4px 15px;box-sizing:border-box;"><section style="color: rgb(255, 255, 255); text-align: center;"><strong data-brushtype="text"><span leaf=""><span textstyle="">二、医生支招：如何科学选择产前诊断遗传检测技术？</span></span></strong></section></section></section></section></section><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><br></span></strong></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">面对多种检测技术，准父母无需盲目纠结，结合自身情况和医生建议选择即可，核心原则如下：</span></span></strong></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><br></span></strong></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">1. 常规筛查优选组合：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">染色体核型分析联合CMA或CNV-Seq，可同时覆盖宏观染色体异常和微小片段病变，实现全面筛查。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">2. 焦虑情绪明显者：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">若主要担心21三体、18三体等常见染色体疾病，且希望快速获取结果，可选择“核型分析+CMA/CNV-Seq+FISH”组合，兼顾全面性与时效性，及时缓解焦虑。</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span style="background-color:#dbeef3;"><strong><span leaf=""><span textstyle="" style="font-size: 16px;">3. 疑难病例精准排查：</span></span></strong></span><span leaf=""><span textstyle="" style="font-size: 16px;">仅当超声提示胎儿结构异常，且前序检测结果均正常时，医生会谨慎建议进行WES检测，避免过度检测。</span></span></p><section style="text-align: center;" nodeleaf=""><span class="wxart_image" wx-style="display:inline-block;width:578px;height:342px;"></span></section><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><span textstyle="" style="font-size: 16px;">产前遗传检测技术的进步，不仅是医学科技的突破，更承载着对生命的敬畏与人文关怀。它让准父母拥有更多知情权，也让医疗服务更具针对性。渭南市妇幼保健院产前诊断团队将以专业的技术、耐心的沟通，为每一个家庭解读生命密码，助力准父母科学守护宝宝的健康起点，让每一份期待都能圆满落地。</span><span textstyle="" style="font-size: 16px;font-weight: bold;">【妇幼健康科普】</span></span></p><p style="text-align: justify; margin-top: 4px; margin-bottom: 4px; line-height: 1.75; color: rgb(51, 51, 51); text-shadow: none; letter-spacing: 1.5px; font-size: 14px; text-indent: 2.21428em;"><span leaf=""><br></span></p><section data-role="outer" label="edit by 135editor" data-pm-slice="0 0 []"><section data-tools="135编辑器" data-id="140195"><section style="margin: 10px auto; padding-top: 20.1%; box-sizing: border-box;"><section style="border: 1px solid #4687ff;border-radius: 10px 10px 0 0;border-bottom: none;box-sizing:border-box;"><section style="width: 50%; margin-top: -20.1%; margin-right: auto; margin-left: auto; box-sizing: border-box; max-width: 50% !important;" data-width="50%"><section style="border-radius: 100%;line-height: 0;padding: 5px;border: 1px solid #4687ff;background-color: #d3e1fa;box-sizing:border-box;"><section style="border-radius: 100%;border: 1px solid #ffffff;box-sizing:border-box;" nodeleaf=""><span class="wxart_image" wx-style="display:inline-block;width:274px;display:block;border-radius:100%;vertical-align:baseline;box-sizing:border-box;max-width:100% !important;height:271px;"></span></section></section></section></section><section style="border: 1px solid #4687ff;border-radius: 0 0 10px 10px;border-top: none;padding: 10px 10px 10px;box-sizing:border-box;"><section><section style="display: flex;justify-content: center;"><section style="background-color: #4687ff;border-radius: 0 10px 0 10px;padding: 6px 20px;box-sizing:border-box;"><section style="color: rgb(255, 255, 254); text-align: center;"><strong data-brushtype="text"><span leaf="">乔艳妮</span><span style="color: rgb(51, 51, 51); font-family: "PingFang SC", "Microsoft Yahei", 微软雅黑, "Lucida Grande", "Lucida Sans Unicode", Helvetica, Arial, Verdana, sans-serif; font-size: 14px; font-weight: 400; text-align: start; background-color: rgb(255, 255, 255); float: none; display: inline !important;" data-pm-slice="0 0 []"><span leaf=""><br></span></span></strong></section></section></section></section><section><section style="width: 23px;box-sizing:border-box;"><svg viewBox="0 0 36.99 26.59" style="display: block;"><g data-name="图层 2"><g data-name="组 67"><path data-name="椭圆 1606-2" d="M23,14A11,11,0,0,1,34,3h0" style="fill:none;stroke:#ffd128;stroke-width:6px;"></path><rect data-name="矩形 1605" x="20" y="12.59" width="14" height="14" style="fill:#ffd427;"></rect><path data-name="椭圆 1606" d="M3,14A11,11,0,0,1,14,3h0" style="fill:none;stroke:#ffd128;stroke-width:6px;"></path><rect data-name="矩形 1605-2" y="12.59" width="14" height="14" style="fill:#ffd427;"></rect></g></g></svg></section><section data-autoskip="1" style="text-align: justify;line-height:1.75em;letter-spacing: 1.5px;font-size:14px;color:#3f3f3f;background-color: transparent;padding: 10px 5px;box-sizing:border-box;"><p><span style="color: rgb(51, 51, 51); font-family: "PingFang SC", "Microsoft Yahei", 微软雅黑, "Lucida Grande", "Lucida Sans Unicode", Helvetica, Arial, Verdana, sans-serif; letter-spacing: normal; text-align: start; float: none; display: inline !important;" data-pm-slice="0 0 []"><span leaf=""><span textstyle="">渭南市妇幼保健院医学遗传科副主任医师，擅长优生遗传咨询及围产期保健，在产筛高风险咨询、胎儿超声异常咨询、不良孕产史家庭或有遗传病家庭的再生育指导等方面均有丰富的临床经验。</span></span></span></p></section></section></section></section></section></section></section><p style="display: none;"><mp-style-type data-value="3"></mp-style-type></p></div><p></p> 为千万孕产妇筑起更坚实的出生缺陷防控防线。 为民服务，尽职尽责 揭秘生命起点的“守护密码” 为民服务，尽职尽责 多谢分享给大家 自己的健康最重要 需要看专家的朋友们注意了 为民服务，尽职尽责
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