Prenatal Diagnostic Value of Chromosomal Microarray in Fetuses with Nuchal Translucency Greater than 2.5 mm

Table 1

Chromosomal findings in samples with other structural malformations.

Case	MA (years)	NT (mm)	Other malformations	Chromosomal findings
1	33	3.6	VSD	Trisomy 21
2	29	3.3	Short and bending femur	Achondroplasia
3	33	3.6	Multiple malformations	N
4	35	2.7	Holoprosencephaly	Trisomy 13
5	27	3.5	Pedicle syndrome	N
6	28	2.7	CHD	Trisomy 21
7	37	4.8	Omphalocele	Trisomy 18
8	33	4.0	Omphalocele	Trisomy 18
9	33	3.2	Choroid plexus cysts	Trisomy 18
10	37	3.7	Holoprosencephaly	N
11	24	2.9	Situs inversus viscerum, CHD	Monosomy X mosaicism
12	36	7.2	Holoprosencephaly, omphalocele	Trisomy 18
13	33	3.5	Diaphragmatic hernia	N

VSD: ventricular septal defect; CHD: congenital heart disease; N: negative results.