An amniocentesis was done, revealing normal karyotype (46,XX).Screening tests for fetal infections (toxoplasmosis, MNI, rubeola, CMV, herpes, Coxsackie, enterovirus and Chikungunya) were negative.
羊水穿刺显示核型正常（46，xx），胚胎感染筛查试验阴性。
The doctor recommended amniocentesis to check for any genetic abnormalities in the fetus.
医生建议进行羊水穿刺以检查胎儿是否有任何遗传异常。
Amniocentesis is a prenatal test that involves taking a small sample of amniotic fluid for analysis.
羊水穿刺是一种产前检测，涉及取一小部分羊水进行分析。
The amniocentesis procedure carries a small risk of miscarriage.
羊水穿刺手术有一定的流产风险。
Many women opt for amniocentesis to gain more information about the health of their baby.
许多女性选择进行羊水穿刺以获取更多关于宝宝健康状况的信息。
Results from amniocentesis can help parents make informed decisions about their pregnancy.
羊水穿刺的结果可以帮助父母对怀孕做出明智的决定。
Amniocentesis is usually performed between the 15th and 20th week of pregnancy.
羊水穿刺通常在怀孕第15周至第20周之间进行。
The doctor will use ultrasound guidance to perform the amniocentesis procedure.
医生将使用超声波引导来执行羊水穿刺手术。
It's important to discuss the risks and benefits of amniocentesis with your healthcare provider.
与您的医疗提供者讨论羊水穿刺的风险和好处非常重要。
Amniocentesis can provide valuable information about the baby's chromosomes and genetic makeup.
羊水穿刺可以提供有关宝宝染色体和遗传基因的宝贵信息。
Some couples choose not to undergo amniocentesis due to personal beliefs or concerns about the procedure.
一些夫妇由于个人信仰或对该程序的担忧而选择不进行羊水穿刺。
It can be done before birth via chorionic-villus sampling or amniocentesis.
它可以在出生前通过绒毛膜-绒毛取样或羊膜穿刺术完成。
来源: Osmosis - GeneticsThis can also be done prenatally by testing fetal DNA obtained through either chorionic villus sampling or amniocentesis.
这可以在产前通过检测胎儿DNA完成，如绒毛膜绒毛取样或羊膜穿刺术。
来源: Osmosis - GeneticsA karyotype can be done before birth with an amniocentesis or at any time after birth with the blood test.
核型分析在出生前就可以用羊膜穿刺术取样或在出生后采血取样。
来源: Osmosis - GeneticsIn more serious cases, amniocentesis, where a sample is taken directly from the amniotic sac surrounding the fetus, can be performed.
在严重的情况下，需行羊膜穿刺术，即直接从胎儿周围的羊膜囊穿刺取样检查。
来源: Osmosis - NerveAn amniocentesis was done, revealing normal karyotype (46,XX).Screening tests for fetal infections (toxoplasmosis, MNI, rubeola, CMV, herpes, Coxsackie, enterovirus and Chikungunya) were negative.
羊水穿刺显示核型正常（46，xx），胚胎感染筛查试验阴性。
The doctor recommended amniocentesis to check for any genetic abnormalities in the fetus.
医生建议进行羊水穿刺以检查胎儿是否有任何遗传异常。
Amniocentesis is a prenatal test that involves taking a small sample of amniotic fluid for analysis.
羊水穿刺是一种产前检测，涉及取一小部分羊水进行分析。
The amniocentesis procedure carries a small risk of miscarriage.
羊水穿刺手术有一定的流产风险。
Many women opt for amniocentesis to gain more information about the health of their baby.
许多女性选择进行羊水穿刺以获取更多关于宝宝健康状况的信息。
Results from amniocentesis can help parents make informed decisions about their pregnancy.
羊水穿刺的结果可以帮助父母对怀孕做出明智的决定。
Amniocentesis is usually performed between the 15th and 20th week of pregnancy.
羊水穿刺通常在怀孕第15周至第20周之间进行。
The doctor will use ultrasound guidance to perform the amniocentesis procedure.
医生将使用超声波引导来执行羊水穿刺手术。
It's important to discuss the risks and benefits of amniocentesis with your healthcare provider.
与您的医疗提供者讨论羊水穿刺的风险和好处非常重要。
Amniocentesis can provide valuable information about the baby's chromosomes and genetic makeup.
羊水穿刺可以提供有关宝宝染色体和遗传基因的宝贵信息。
Some couples choose not to undergo amniocentesis due to personal beliefs or concerns about the procedure.
一些夫妇由于个人信仰或对该程序的担忧而选择不进行羊水穿刺。
It can be done before birth via chorionic-villus sampling or amniocentesis.
它可以在出生前通过绒毛膜-绒毛取样或羊膜穿刺术完成。
来源: Osmosis - GeneticsThis can also be done prenatally by testing fetal DNA obtained through either chorionic villus sampling or amniocentesis.
这可以在产前通过检测胎儿DNA完成，如绒毛膜绒毛取样或羊膜穿刺术。
来源: Osmosis - GeneticsA karyotype can be done before birth with an amniocentesis or at any time after birth with the blood test.
核型分析在出生前就可以用羊膜穿刺术取样或在出生后采血取样。
来源: Osmosis - GeneticsIn more serious cases, amniocentesis, where a sample is taken directly from the amniotic sac surrounding the fetus, can be performed.
在严重的情况下，需行羊膜穿刺术，即直接从胎儿周围的羊膜囊穿刺取样检查。
来源: Osmosis - Nerve探索常用高频词汇