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Social individual circumstances of the personalized medicine in prevention of the family of fetus anomalies (review of international experience)

摘要

In this work the brief classification of the main of family of fetus anomalies with a correlation of scientic advances in genetics, molecular biology, embryology. The article makes it possible to characterize the current state of development the personalized medicine in the prevention of family of fetus anomalies.

关于作者

A. Kiselev
I.M. Sechenov First MSMU
俄罗斯联邦


参考

1. Wilcox A.J. et al. Folic Acid Supplements and the Risk of Facial Clefts: A National Population-Based Case-Control Study // British Medical Journal? January 26. 2007.

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3. Kerem B., et al Identifi cation of the Cystic Fibrosis Gene: Genetic Analysis/ Science. 2009. vol. 245: 1073-1080.

4. O’Leary V.B., et al MTRR and MTHFR Polymorphism: Link to Down Syndrome // American Journal of Medical Genetics. January 15, 2002, vol. 107: 151-155.

5. Scala I. et al Analysis of seven Maternal Polymorphisms of Genes Involved in Homocysteine // Folate Metabolism and Risk of Down Syndrome. Genetics in Medicine. Vol. 290; 7, july 2006: 409-416.

6. Sherman S. et al. American College of Medical Genetics Practice Guideline: Fragile X Syndrome: Diagnostic and Carrier Testing // Genetics in Medicine. Vol. 7; 8 October 2005: 584-587.

7. Queenan J.T. Noninvasive Prenatal Fetal Rh Genotiping: The Time has Come // Obstetrics and Gynecology. Vol. 1006, number 4, October 2005: 682-685.


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ISSN 2218-7332 (Print)
ISSN 2658-3348 (Online)