2011•Chinese Journal of Birth Health & HeredityRequires access

Prenatal diagnosis in 311 cases of mid-gestation women

Hao Ge-fan

Open publisher page 0 citations

Abstract

Objective: By analizing karyotype with amniotic cavity in mid-gestation women,to explore clinical risk factors of fetal chromosomal abnormalities and improve the understanding of clinical physicians to the prenatal diagnosis indication of karyotype analysis in amniotic fluid.Methods:311 cases women with 16 ~ 30 pregnant weeks undergo amniocentesis monitored by B-orientation.extract amniotic fluid to culture,and performed the G-banding staining for karyotype analysis.Results:13 cases of chromosomal abnormalities were diagnozied,accounting for 4.18%.Among them,5 cases in pregnant woman or her spouse(5 / 6),6 cases in advanced-age pregnant women(4 / 161),1 case in the women with a reproductive history of 21-or 18 trisomy(1 / 30),2 cases in women under 35 years old and with a history of high risk of Down syndrome(2 / 87),1 case in women with a reproductive history of deformed children.No cases were found in women with positive results of ultrasound soft targets and neither in volunteers without prenatal diagnosis indications.Conclusions: It′s effictive for diagnozed fetal chromosomal disease using amniotic fluid sample to analizing chromosome.The high risks for fetal chromosomal abnormalities include the spouses with chromosomal abnormalities,advanced age pregnant woman,hish-risk woman with Down syndrome,a reproductive history of aneuploid children and deformed children,and positive results of ultrasound soft targets.It′s important to pay highly attention to these risks.

About this research paper

What this paper is about

Objective: By analizing karyotype with amniotic cavity in mid-gestation women,to explore clinical risk factors of fetal chromosomal abnormalities and improve the understanding of clinical physicians to the prenatal diagnosis indication of karyotype analysis in amniotic fluid.Methods:311 cases women with 16 ~ 30 pregnant weeks undergo amniocentesis monitored by B-orientation.extract amniotic fluid to culture,and performed the G-banding staining for karyotype analysis.Results:13 cases of chromosomal abnormalities were diagnozied,accounting for 4.18%.Among them,5 cases in pregnant woman or her spouse(5 / 6),6 cases in advanced-age pregnant women(4 / 161),1 case in the women with a reproductive history of 21-or 18 trisomy(1 / 30),2 cases in women under 35 years old and with a history of high risk of Down syndrome(2 / 87),1 case in women with a reproductive history of deformed children.No cases were found in women with positive results of ultrasound soft targets and neither in volunteers without prenatal diagnosis indications.Conclusions: It′s effictive for diagnozed fetal chromosomal disease using amniotic fluid sample to analizing chromosome.The high risks for fetal chromosomal abnormalities include the spouses with chromosomal abnormalities,advanced age pregnant woman,hish-risk woman with Down syndrome,a reproductive history of aneuploid children and deformed children,and positive results of ultrasound soft targets.It′s important to pay highly attention to these risks.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective: By analizing karyotype with amniotic cavity in mid-gestation women,to explore clinical risk factors of fetal chromosomal abnormalities and improve the understanding of clinical physicians to the prenatal diagnosis indication of karyotype analysis in amniotic fluid.Methods:311 cases women with 16 ~ 30 pregnant weeks undergo amniocentesis monitored by B-orientation.extract amniotic fluid to culture,and performed the G-banding staining for karyotype analysis.Results:13 cases of chromosomal abnormalities were diagnozied,accounting for 4.18%.Among them,5 cases in pregnant woman or her spouse(5 / 6),6 cases in advanced-age pregnant women(4 / 161),1 case in the women with a reproductive history of 21-or 18 trisomy(1 / 30),2 cases in women under 35 years old and with a history of high risk of Down syndrome(2 / 87),1 case in women with a reproductive history of deformed children.No cases were found in women with positive results of ultrasound soft targets and neither in volunteers without prenatal diagnosis indications.Conclusions: It′s effictive for diagnozed fetal chromosomal disease using amniotic fluid sample to analizing chromosome.The high risks for fetal chromosomal abnormalities include the spouses with chromosomal abnormalities,advanced age pregnant woman,hish-risk woman with Down syndrome,a reproductive history of aneuploid children and deformed children,and positive results of ultrasound soft targets.It′s important to pay highly attention to these risks.

Key concepts: Amniocentesis, Obstetrics, Amniotic fluid, Prenatal diagnosis, Medicine, Trisomy, Spouse, Advanced maternal age

Related papers

Back to paper searchBrowse research topicsOriginal source
Prenatal diagnosis in 311 cases of mid-gestation women — Research Paper | ScholarLens