Ultrasound evaluation of fetal chromosome disorders
Küçük Resim Yok
Tarih
2007
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Turkish Soc Radiology
Erişim Hakkı
info:eu-repo/semantics/closedAccess
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.
Açıklama
Anahtar Kelimeler
ultrasonography, nuchal translucency measurement, nasal bone, nuchal skin-fold thickness
Kaynak
Diagnostic and Interventional Radiology
WoS Q Değeri
N/A
Scopus Q Değeri
Q2
Cilt
13
Sayı
2
