Diagnosis by Prenatal Testing
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概要
- 論文の詳細を見る
Along with our culture and religion, the lack of major genetic diseases in Japan, such as the β thalasemia found in the Mediterranean, cystic fibrosis in Caucaseans and sickle cell anemia in Africans, has possibly contributed to the relatively limited official debata on genetic testing and prevention of genetic diseases. However, the recent expansion of knowledge regarding genetic and reproductive procedures has brought to light a new aspect of biomedical ethics, a condition that necessarily has become a subject of wide and official discussion, even in our country. The most effective force for serious debate has been the issue of maternal serum marker testing for chromosomal abnormalities. The American Academy of Pediatrics and College of Obstetrics and Gynecology stated that testing should be recommended for pregnant women under 35 years in the guidelines for perinatal care in 1997. Our general opinion is that such testing should be carried out only on a voluntary basis. However, insufficient informed decision making and a shortage of scientific evaluation of the testing have given rise to concern by Japan Society of Human Genetics and Parents' Society of Down Syndrome and others. Recently, the National Council of Health and Welfare proposed guidelines for maternal serum marker tests.
- 社団法人日本産科婦人科学会の論文
- 2000-02-01
著者
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SUZUMORI Kaoru
Department of Obstetrics and Gynecology, Nagoya City University Medical School
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Suzumori Kaoru
Deparatment Of Obstetrics And Gynecology Nagoya City University Medical School
関連論文
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- Maternal uniparental disomy of chromosome 16 in a case of spontaneous abortion
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- Pharmacokinetic and pharmacodynamic anakysis of combined chemotherapy with carboplatin and paclitaxel for patients with ovarian cancer
- IS-21 Analysis of BRCA1 Gene Deletion in Japanese Ovarian Cancer by FISH
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- Low dose gonadotropin-releasing hormone agonist treatments with early discontinuation for controlled ovarian hyperstimulation in an in vitro fertilization program
- Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis : Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies
- Parental origin and cell stage of non-disjunction of double trisomy in spontaneous abortion
- Mutation analysis of the BRCA1 gene in 76 Japanese ovarian cancer patients : four germline mutations, but no evidence of somatic mutation
- Molecular Genetic Techniques for Prenatal Diagnosis
- PRENATAL DIAGNOSIS AND FETAL TREATMENT : Early diagnosis and treatment of congenital anomalies
- Infertility and assisted reproductive technologies : Bright and dark sides
- Incidence and types of congenital cardiovascular malformations in Japanese trisomy 21 fetuses around 20 weeks
- Diagnosis by Prenatal Testing
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- CA125 and UQCRFS1 FISH studies of ovarian carcinoma(Session4 Oncology4)
- Pharmacokinetic and pharmacodynamic analysis of combined chemotherapy with carboplatin and cyclophosphamide in patients with gynecological cancers
- Cardiac failure caused by severe pre-eclampsia with placental abruption, and its treatment with anti-hypertensive drugs
- Cytogenetic Effects of Cryopreservation on Human Sperm : Assessment Using an Improved Method for Analyzing Human Sperm Chromosomes
- Prenatal diagnosis as a test for genodermatoses : its past, present and future