Journal of International Reproductive Health/Family Planning ›› 2013, Vol. 32 ›› Issue (6): 433-437.

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Prenatal Diagnosis of Single-Gene Defects

YAN Kai,JIN Fan   

  1. Department of Reproductive and Genetics, Women′s Hospital, Zhejiang University; Key Laboratory of Reproductive and Genetics, Ministry of Education, Hangzhou 310006, China.
  • Received:1900-01-01 Revised:1900-01-01 Published:2013-11-15 Online:2013-11-15
  • Contact: JIN Fan

Abstract: Single-gene defects, which has the unfavorable prognosis, is the main cause of the newborn's defect. Couples can prevent birth of child carrying the same genetic disorder with the proband. Currently, the prenatal diagnosis contains preimplantation genetic diagnosis and trimester prenatal diagnosis. Traditional invasive prenatal diagnosis acquire specimens from fetal relying on surgery. It is accurate, but with a certain risk of miscarriage. The new method of prenatal diagnosis (such as preimplantation genetic diagnosis and non-invasive prenatal diagnosis) and the traditional way are complementary to one another. In this review, we discuss the progress of prenatal diagnosis of Single-gene defects and the significance of genetic counseling in order to provide some ideas in clinical practice.

Key words: Genetic diseases, inborn, Prenatal diagnosis, Preimplantation diagnosis, Genes, Genetic counseling, Single-gene defects