doctors diagnosed the fetus with triploidy during the routine ultrasound scan.
医生在常规超声扫描中诊断出胎儿患有三倍体。
triploidy is a rare chromosomal abnormality characterized by three sets of chromosomes.
三倍体是一种罕见的染色体异常，其特征是具有三组染色体。
the patient decided to terminate the pregnancy after receiving the triploidy diagnosis.
在收到三倍体诊断结果后，患者决定终止妊娠。
most cases of triploidy result in spontaneous miscarriage during the first trimester.
大多数三倍体病例会导致第一孕期自然流产。
genetic counseling is recommended for parents to understand the causes of triploidy.
建议父母接受遗传咨询，以了解三倍体的成因。
distinguishing between partial molar pregnancy and triploidy requires careful histopathological examination.
区分部分性葡萄胎和三倍体需要仔细的组织病理学检查。
pathologists identified triploidy as the cause of the intrauterine fetal demise.
病理学家确认三倍体是导致胎儿宫内死亡的原因。
the prognosis for live birth is extremely poor for fetuses with complete triploidy.
完全三倍体胎儿的活产预后极差。
advanced maternal age is not considered a significant risk factor for triploidy.
高龄产妇不被认为是三倍体的显著危险因素。
distinctive physical malformations often suggest the presence of triploidy in the fetus.
独特的身体畸形通常提示胎儿存在三倍体。
karyotyping confirmed the presence of 69 chromosomes indicating triploidy syndrome.
核型分析证实了69条染色体的存在，表明为三倍体综合征。
prenatal screening tests can sometimes indicate potential risks for triploidy.
产前筛查测试有时可以提示三倍体的潜在风险。
doctors diagnosed the fetus with triploidy during the routine ultrasound scan.
医生在常规超声扫描中诊断出胎儿患有三倍体。
triploidy is a rare chromosomal abnormality characterized by three sets of chromosomes.
三倍体是一种罕见的染色体异常，其特征是具有三组染色体。
the patient decided to terminate the pregnancy after receiving the triploidy diagnosis.
在收到三倍体诊断结果后，患者决定终止妊娠。
most cases of triploidy result in spontaneous miscarriage during the first trimester.
大多数三倍体病例会导致第一孕期自然流产。
genetic counseling is recommended for parents to understand the causes of triploidy.
建议父母接受遗传咨询，以了解三倍体的成因。
distinguishing between partial molar pregnancy and triploidy requires careful histopathological examination.
区分部分性葡萄胎和三倍体需要仔细的组织病理学检查。
pathologists identified triploidy as the cause of the intrauterine fetal demise.
病理学家确认三倍体是导致胎儿宫内死亡的原因。
the prognosis for live birth is extremely poor for fetuses with complete triploidy.
完全三倍体胎儿的活产预后极差。
advanced maternal age is not considered a significant risk factor for triploidy.
高龄产妇不被认为是三倍体的显著危险因素。
distinctive physical malformations often suggest the presence of triploidy in the fetus.
独特的身体畸形通常提示胎儿存在三倍体。
karyotyping confirmed the presence of 69 chromosomes indicating triploidy syndrome.
核型分析证实了69条染色体的存在，表明为三倍体综合征。
prenatal screening tests can sometimes indicate potential risks for triploidy.
产前筛查测试有时可以提示三倍体的潜在风险。
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