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Table 1 Clinical features in fetuses with Williams-Beuren syndrome

From: Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis

Case number

Maternal age (years)

GA (weeks)

Ultrasound findings

CMA results

Size

Outcome

1

31

23

MCDK

arr7q11.23(72723370–74154209)×1

1.43

TOP

2

27

33

AC

arr7q11.23(72624203–74154497)×1

1.53

TOP

3

29

30

DA

arr7q11.23(72718277–74143060)×1

1.42

Lost to follow-up

4

34

22

TOF, SVAS, RAA

arr7q11.23(72718277–74142190)×1

1.42

TOP

5

38

33

VSD, AC

arr7q11.23(72718278–74143030)×1

1.42

TOP

6

33

31

PAS, IUGR

arr7q11.23(72557180–74628840)×1

2.07

TOP

7

23

27

IUGR

arr7q11.23(72701099–74136633)×1

1.44

TOP

8

32

24

VSD

arr7q11.23(72723371–74141494)×1

1.42

TOP

  1. GA gestational age, CMA chromosome microarray, MCDK multicystic dysplastic kidney, AC aortic coarctation, DA duodenal atresia, TOF Tetralogy of Fallot, SVAS supravalvular aortic stenosis, RAA right aortic arch, VSD ventricular septal defect, PAS pulmonary artery stenosis, IUGR intrauterine growth retardation, TOP termination of pregnancy