A pilot study was performed to determine the incidence of congenital h
ypothyroidism (CH) in Turkey and to build a model for nationwide scree
ning. From December 1991 to December 1992, 30097 newborns were screene
d for CH using a primary measurement of thyroid stimulating hormone in
capillary blood on days 3-5 of life. Samples were obtained in collabo
ration with the ongoing nationwide phenylketonuria screening programme
. Eleven cases of primary CH were detected giving the incidence of 1:2
736. Recall rate was 2.3%. Replacement therapy with L-thyroxine was st
arted after the confirmation of diagnosis. The median age at the initi
ation of replacement therapy was 23 days (range 7-35 days). Conclusion
The incidence of CH is notably higher in Turkey than reported in most
other countries. Iodine deficiency and/or dyshormonogenesis might con
tribute to this high incidence. This result emphasizes the necessity o
f a nationwide screening programme.