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. 2017 Jun 2;68(3):197–203. doi: 10.1007/s13224-017-1011-6

Table 2.

Systemwise structural malformations in NIHF cases

Causes No of cases %
CNS 10 7.7
Anencephaly 1 0.8
Hydrocephalus 3 2.3
Microcephaly 2 1.5
Dandy walker malformation 3 2.3
Agenesis of corpus callosum 1 0.8
CVS 34 26.1
Structural heart defect 21 16.1
Rhythm disturbance 6 4.6
Cardiomegaly 7 5.4
Neck and thorax 19 14.6
Cystic hygroma 15 11.5
Thoracic duplication cyst 1 0.8
CCAM 3 2.3
GIT 7 5.4
Echogenic bowel 5 3.8
Intraabdominal varix 1 0.8
Omphalocele 1 0.8
Musculoskeletal skeletal 11 8.5
Osteogenesis Imperfecta 1 0.8
Asphixiating thoracic dysplasia 2 1.5
Short long bones 2 1.5
Fetal akinesia syndrome 6 4.6
Renal 5 3.8
Hydronephrosis 2 1.5
LUTO 2 1.5
MCK 1 0.8
Twin complications 4 3.1
TTTS 3 2.3
TRAP 1 0.8
No abnormality on US 36 27.7
Anemia—MCA PSV 4 3.1
Total 130 100

P value of less than 0.05 is taken as significant and is marked in bold

CNS central nervous system, CVS cardiovascular system, CCAM congenital cystic adenomatoid malformation of lung, TTTS twin–twin transfusion syndrome, TRAP twin reversed arterial perfusion, URSM urorectal septal malformation, MCA PSV middle cerebral artery peak systolic velocity