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3-032, 3-05d. [ edit on Wikidata] Obstetric ultrasonography, or prenatal ultrasound, is the use of medical ultrasonography in pregnancy, in which sound waves are used to create real-time visual images of the developing embryo or fetus in the uterus (womb). The procedure is a standard part of prenatal care in many countries, as it can provide a ...
The first, second, combined, and third trimester screens typically consist of an ultrasound (abdominal and/or transvaginal) and maternal blood/serum testing. The ultrasound is used to visually assess the growth, development, and activity of the fetus through imaging observations and measurements.
The second trimester is defined as starting, between the beginning of week 13 (12 weeks +0 days of GA) [4] and beginning of week 15 (14 weeks + 0 days of GA). [36] It ends at the end of week 27 (26 weeks + 6 days of GA) [ 36 ] or end of week 28 (27 weeks + 6 days of GA).
The embryonic and prenatal development of the male reproductive system is the process whereby the reproductive organs grow, mature and are established. It begins with a single fertilized egg and culminates 38 weeks later with the birth of a male child. It is a part of the stages of sexual differentiation.
The human fetus moves throughout its entire development. Fetal movement refers to motion of a fetus caused by its own muscle activity. Locomotor activity begins during the late embryological stage and changes in nature throughout development. Muscles begin to move as soon as they are innervated. These first movements are not reflexive, but ...
Cephalic presentation. In obstetrics, a cephalic presentation or head presentation or head-first presentation is a situation at childbirth where the fetus is in a longitudinal lie and the head enters the pelvis first; the most common form of cephalic presentation is the vertex presentation, where the occiput is the leading part (the part that ...
When an echogenic intracardiac focus is identified in an otherwise normal second trimester fetus, a normal cell-free DNA test can be very reassuring and obviate the need for invasive testing. Amniocentesis is a test to check a baby's chromosomes. A small amount of amniotic fluid, which contains some fetal cells, is removed and tested.
In another study values of 79.6% and 2.7% for the combined screening were then improved with the addition of second trimester ultrasound scanning to 89.7% and 4.2% respectively. [13] A further study reported detection of 88% for trisomy 21 (Down syndrome) and 75% for trisomy 18 (Edwards syndrome), with a 3.3% false-positive rate. [14]