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. Author manuscript; available in PMC: 2015 Sep 1.
Published in final edited form as: Am J Med Genet A. 2014 Jun 16;164(9):2250–2255. doi: 10.1002/ajmg.a.36638

Table II.

Association between hepatoblastoma and congenital anomalies

Variable of Interest Controls (%)
N=387
Cases (%)
N=367
OR (CI) Fisher’s p-value
Cleft lip or palate 1 (0.3) 1 (0.3) 1.05 (0.07, 16.9) 1.00
Spina bifida or other spinal defect 2 (0.5) 4 (1.1) 2.12 (0.39, 11.7) 0.44
Large/multiple birthmarks 30 (7.8) 37 (10.1) 1.33 (0.81, 2.21) 0.31
Trisomy 18 0 (0.0) 1 (0.3) - 0.49
Other genetic conditions 1 (0.3) 2 (0.5) 2.11 (0.19, 23.4) 0.61
Down syndrome 1 (0.3) 0 (0.0) - 1.00
Rib abnormalities 0 (0.0) 1 (0.3) - 0.49
Small head/microcephaly 0 (0.0) 3 (0.8) - 0.11
Kidney, bladder, sex organ abnormality 6 (1.6) 18 (4.9) 4.75 (1.74, 13.0) 0.01
 Hypospadias* 2 (0.5) 4 (1.1) 2.1 (0.38, 11.4) 0.44
 Any kidney/bladder* 3 (0.8) 12 (3.3) 4.3 (1.2, 15.3) 0.02
 Sex organ* 5 (1.3) 6 (1.6) 1.24 (0.37, 4.1) 0.77
*

Controlled for sex (Ref=Male)