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WS 322.1-2010 PDF English

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WS 322.1-2010English399 Add to Cart 3 days [Need to translate] Technical standards of prenatal screening and diagnosis for fetal common chromosomal abnormalities and open neural tube defects. Part 1: Maternal serum prenatal screening in second trimester

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Basic data

Standard ID WS 322.1-2010 (WS322.1-2010)
Description (Translated English) Technical standards of prenatal screening and diagnosis for fetal common chromosomal abnormalities and open neural tube defects. Part 1: Maternal serum prenatal screening in second trimester
Sector / Industry Health Industry Standard
Classification of Chinese Standard C59
Classification of International Standard 11.020
Word Count Estimation 10,122
Date of Issue 2010-06-08
Date of Implementation 2010-12-31
Quoted Standard WS/T 247; WS/T 250
Regulation (derived from) ?Health-Communication (2010) 17; Industry Standard Filing Announcement 2010 No.7 (Total No.127)
Issuing agency(ies) National Health and Family Planning Commission of the People's Republic of China
Summary This standard specifies the parent trimester prenatal serologic screening procedures, informed consent, screening data and specimen collection, laboratory testing, informed of the outcome and treatment for high-risk pregnant women and followed up requirements. This section applies to the time of birth below the age of 35 pregnant women in the second trimester of fetal common chromosomal abnormalities (Down's syndrome and 18-trisomy) serum and open neural tube defects school prenatal screening.

WS 322.1-2010: Technical standards of prenatal screening and diagnosis for fetal common chromosomal abnormalities and open neural tube defects. Part 1: Maternal serum prenatal screening in second trimester







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Technical standards of prenatal screening and diagnosis for fetal common chromosomal abnormalities and open neural tube defects. Part 1. Maternal serum prenatal screening in second trimester ICS 11.020 C59 Record number. 29140-2010 People's Republic of China health industry standards Fetal common chromosomal abnormalities and openness Prenatal screening and diagnostic criteria for neural tube defects Part 1. Prenatal screening of maternal serology in pregnancy Technical standards of prenatalscreeninganddiagnosisfor Part 1. Maternalserumprenatalscreeninginsecondtrimester 2010-06-08 released 2010-12-31 implementation Ministry of Health of People's Republic of China released

Foreword

WS 322 "Prenatal screening and diagnostic techniques for common chromosomal abnormalities in the fetus and open neural tube defects" is now published as follows section. --- Part 1. prenatal screening of maternal serology in the second trimester; --- Part 2. Fetal common chromosomal abnormalities cytogenetic prenatal diagnostic criteria. This part is the first part of WS 322. This part of the Appendix A is informative, Appendix B is a normative appendix. This section proposed by the Ministry of Health Medical Services Standards Committee. This part of the People's Republic of China Ministry of Health approval. This section mainly drafted by. Chinese Academy of Medical Sciences Beijing Union Medical College Hospital, Yunnan First People's Hospital, Sichuan University, West China Second Medical Hospital, Zhejiang University School of Medicine Obstetrics and Gynecology Hospital. The main drafters of this section. Bian Xuming, Zhu Baosheng, Liu Juntao, Wang and Lv Shiming, Ma Liangkun, Jiang Yu Lin, Qi Qing Wei, Xia Jiahui, Sun nirvana. Fetal common chromosomal abnormalities and openness Prenatal screening and diagnostic criteria for neural tube defects Part 1. Prenatal screening of maternal serology in pregnancy

1 Scope

WS 322 provisions of this part of the maternal serological prenatal screening program, informed consent, screening materials and specimens collected Set, laboratory tests, notification of results and treatment and follow-up of high-risk pregnant women. This section applies to childbirth at the age of 35 pregnant women in the second trimester of pregnancy common chromosomal abnormalities (Down's syndrome and 18-trisomy syndrome) and serological prenatal screening of open neural tube defects.

2 Normative references

The following documents for the application of this document is essential. For dated references, only the dated version applies to this article Pieces. For undated references, the latest edition (including all amendments) applies to this document. WS/T 247 alpha fetoprotein detection of prenatal monitoring and open guidelines for the diagnosis of neural tube defects WS/T 250 clinical laboratory quality assurance requirements

3 Terms and definitions

The following terms and definitions apply to this document. 3.1 Common fetal chromosomal abnormalities commonchromosomeabnormalities Chromosomal disorders are the most common genetic disorder that causes birth defects in newborns. About 400 kinds of chromosomal diseases, of which common There are more than 60 species, the major chromosomal abnormalities are 21-trisomy (Down's Syndrome), 18-trisomy and 13-trisomy and sex-stained Body abnormalities, followed by chromosomal abnormalities. 3.2 Open neural tube defects in openneuraltubedefects 4 weeks pregnant embryo neural tube is not closed, according to the location of the defect and the clinical manifestations of different severity of open neural tube defects Including anencephaly and open spina bifida, the former is fatal and can lead to miscarriage, stillbirth or stillbirth, the latter can be paralyzed and incontinent Other symptoms. 3.3 During pregnancy, thesecondtrimester Pregnancy 13 weeks ~ 20 6 weeks, the screening time during pregnancy usually refers to 15 weeks pregnant to 20 6 weeks. 3.4 Prenatal screening prenatalscreening Through the simple, economical and less traumatic testing methods, some fetuses with congenital defects and genetic diseases are found in the pregnant women group High-risk pregnant women, in order to further confirm the diagnosis.
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