科室简介
产前诊断专科
提供常见遗传病、染色体病、胎儿宫内感染等的检查、咨询、诊断等医疗服务。我中心1994年开展介入性产前诊断工作，穿刺成功率为99.9%。绒毛穿刺术术后流产率为0.1%，羊膜腔穿刺术术后流产率为0.05%，脐静脉穿刺术术后流产率为0.3%，远低于世界报道的1%的风险值。以2014年为例，中心全年完成675例绒毛取材术、5306例羊膜腔穿刺术、812例脐静脉穿刺术；进行了110例羊水置换术、63例胎儿腹水穿刺、15例减胎术。
胎儿保健专科
指导育龄夫妇进行优生优育的准备，特别是针对高龄和不良生育史的人群。指导孕期营养，指导在特定时间进行产前检查，制定个性化的妊娠监督。进行双胎、多胎孕妇孕期监测、预后评估并及时进行干预性治疗。可对多胎妊娠进行选择性的减胎术，对双胎之一异常、双胎输血综合征、sIUGR和Trap等复杂性双胎制定个性化的妊娠监督方案。
地中海贫血咨询门诊
提供地中海贫血知识的咨询、宣教、检查等医疗服务，对常见及罕见类型的地中海贫血进行诊断，指导优生优育。
复发性流产专科
我中心于2007年开展免疫治疗至今，对复发性流产的诊治积累了丰富的经验。每年进行治疗约3300人次，经治疗，封闭抗体转阳率达80～85%，治疗后妊娠成功率达60～70%。
小儿遗传专科
对智力低下、语言异常、听力异常、行为异常、代谢异常和发育迟缓的患者进行评估、原因查找和个性化治疗方案的设计，指导夫妇科学妊娠。
Out patient service
Prenatal diagnosis
We provide counseling, medical examinations and diagnosis for common genetic diseases, chromosome disorders and Intrauterine infection. We have applied advanced technique and rich experience in invasive prenatal diagnosis. In 2012, we performed 675 cases of Chorionic Villus Sampling, 5306 cases of amniocenteses, 812 umbilical cord blood sampling, 110 cases of amniotic fluid replacement, 63 cases of fetal ascites paracentesis, and 15 cases of multifetal pregnancy reduction.
Fetus health care
We provided professional recommendation to people in childbearing age, especially the advanced maternal age couples with abnormal reproductive history. We provide clinic service and laboratory tests to monitor the situation of maternal and fetal health. We will provide treatment if the patient are multiple pregnancy, twin-to-twin transfusion syndrome, intrauterine growth retardation etc.
Thalassemia
Thalassemia health education and genetic counseling for couples with childbearing age, and detection for gene mutations of Thalassemia.
Recurrent spontaneous abortion
We have several experts on the diagnosis and treatment of recurrent spontaneous abortion. We provide clinical service to about 3,300 patients each year, and about 70% of patients got successful pregnancy after immunotherapy.
Pediatrics genetics
We provide assessment, counseling and personalized treatment programs for Children with mental retardation, abnormal language development, hearing loss, abnormal behavior, metabolic disorder, and/ or developmental delay.
