Conţinutul numărului revistei |
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Articolul urmator |
1227 37 |
Ultima descărcare din IBN: 2023-04-20 19:54 |
Căutarea după subiecte similare conform CZU |
618.3-037-073.48+076+576.3 (1) |
Științe medicale. Medicină (10970) |
ȘTIINȚĂ ȘI CUNOȘTINȚE. ORGANIZARE. ȘTIINȚA CALCULATOARELOR. INFORMARE. DOCUMENTARE. BIBLIOLOGIE. INSTITUȚII. PUBLICAȚII (10231) |
Biologie celulară și subcelulară. Citologie (129) |
SM ISO690:2012 MOŞIN, Veaceslav, HOTINEANU, Alina, CREŢU, Adrian, CERTAN-BEJAN, Rodica, MOŞIN, Veaceslav Jn., BOLOGAN, Ion. Metode de screening genetic prenatal. Testele dublu, triplu şi cvadruplu. In: Buletin de Perinatologie, 2016, nr. 1(69), pp. 119-127. ISSN 1810-5289. |
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Buletin de Perinatologie | |||||||
Numărul 1(69) / 2016 / ISSN 1810-5289 | |||||||
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CZU: 618.3-037-073.48+076+576.3 | |||||||
Pag. 119-127 | |||||||
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Rezumat | |||||||
Antenatal screening of the hereditary diseases and congenital malformations during the first and second trimester of pregnancy is an important tool for evaluation of intrauterine fetal condition. Special attention is paid to the principles of antenatal screening organization, echographic markers and biochemical methods of fetal development assessment. Antenatal genetic screening includes fetal ultrasound and biochemical screening (estimation of certain plasmatic markers, which fl uctuate in cases of certain fetal diseases). There are several types of screening (depending on number of performed biochemical tests): double test (combined test), triple test and quadruple test. Screening tests are not pretending to be the source of the final diagnosis. They rather give a possibility to identify the group of pregnant with an increased risk of certain fetal pathologies, which require specifi c diagnostic methods. The current recommendations are presented for general practitioners, gynaecologists, specialist in genetics and for patients. |
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Cuvinte-cheie antenatal screening, double test, triple test, ecography, fetal malformations, Down syndrome, pregnancy |
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