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Arch Dis Child Fetal Neonatal Ed 90:F69-F72 doi:10.1136/adc.2003.039065
  • Original article

Contribution of genetic factors to neonatal transient hypothyroidism

Table 2

 Clinical and laboratory findings in babies with neonatal transient hypothyroidism with or without the 2268insT mutation, and in 20 control subjects

No M/F GA<38 weeks FH TSH* ⩾80 μU/ml T4* <25.8 nmol/l AB TSH†(μU/ml) T4† (nmol/l)
Values of TSH and T4 are mean (SD); all other values are numbers of affected/non-affected. p Values are for comparisons between 2268insT(+) and 2268insT(−). Comparisons of differences among three groups, p<0.0001 for TSH; p  =  0.409 for T4.
*Measured at initial confirmatory diagnosis; †measured after T4 withdrawal.
M/F, Males/females; GA, gestational age; FH, positive family history; TSH, thyroid stimulating hormone; AB, antibody; T4, thyroxine.
2268insT(+) 10 6/4 1/10 4/10 7/10 3/10 0/8 4.29 (1.65) 105.3 (20.9)
2268insT(−) 82 42/40 9/82 15/62 32/82 26/82 3/75 4.36 (2.12) 110.3 (20.1)
p Value 0.74 0.9 0.26 0.9 1.0 0.12 0.95 0.47
Controls 20 11/9 2.04 (1.14) 103.7 (13.4)

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