Ultrasound evaluation of fetal chromosome disorders


Tamsel S. , Oezbek S. S. , DEMIRPOLAT G.

DIAGNOSTIC AND INTERVENTIONAL RADIOLOGY, cilt.13, ss.97-100, 2007 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 13 Konu: 2
  • Basım Tarihi: 2007
  • Dergi Adı: DIAGNOSTIC AND INTERVENTIONAL RADIOLOGY
  • Sayfa Sayısı: ss.97-100

Özet

Prenatal diagnosis of chromosomal disorders requires an invasive test in women regarded as being at high risk after screening. There is extensive evidence that effective screening for major chromosomal abnormalities can be provided in the first and second trimesters of pregnancy. With the association of some biochemical markers, it is possible to identify about 90% of chromosomal abnormalities. In this article, we aimed to review the important ultrasonographic markers of chromosomal abnormalities, including nuchal translucency, nasal bone and nuchal skin-fold thickness, based on the data available in the literature.