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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 III.

Association between hepatoblastoma and congenital anomalies in Utah Population Database

Variable of Interest Controls (%)
N=290
Cases (%)
N=29
OR (CI)* Fisher’s p-value
Cleft lip or palate 0 (0.0)% 0 (0.0)% -- --
Spina bifida 0 (0.0)% 0 (0.0)% -- --
Large/multiple birthmarks 1 (0.3)% 0 (0.0)% 1.0
Trisomy 18 0 (0.0)% 0 (0.0)% -- --
Other genetic conditions 0 (0.0)% 0 (0.0)% -- --
Down syndrome 1 (0.3)% 0 (0.0)% -- 1.0
Rib abnormalities 1 (0.3)% 1 (3.4)% 4.3 (0.23, 80.0) 0.17
Small head/microcephaly 0 (0.0)% 0 (0.0)% -- --
Kidney, bladder, sex organ abnormalities 2 (0.7)% 3 (10.3)% 12.0 (1.61, 89.6) 0.006
 Hypospadias 1 (0.3)% 0 (0.0)% <0.001 (n/a) 1.0
 Any kidney/bladder 0 (0.0)% 2 (6.9)% >99 (n/a) 0.008
 Sex organ anomalies 1 (0.3)% 1 (3.4)% 25.7 (1.63, >99) 0.02
Heart or pulmonary anomalies 2 (0.7)% 2 (6.9)% 7.4 (0.87, 62.7) 0.04
*

Controls were matched 10:1 to cases on sex and birth year; model covariates include birth weight, maternal age, and maternal education.