microcephaly and mental impairmentor retardation. Depending on the dose, dose rate

and period of gestation, the severity of these effects may range fromclinically
undetectable, or insignificant, some degree of disability, to incompatibility with intrauterine

or neonatallife. Although the threshold for specific end points may be greater, the
overall risk to the embryo or fetus of exposure at any time during gestation does not

appear to be increased below a threshold of 50 mGy (29).
3.3

Stochastic Effects

Experimental and epidemiological studies have contributed an extensive body of
knowledge about radiogenic stochastic effects. The clinical outcomes are not unique to
radiation. Their association with radiation has been established only by observation among
a numberofirradiated populations of disease rates that increase significantly with
increasing dose. It currently is not possible to unequivocally attribute specific outcomes in
individuals to their exposure to radiation. Relationships between specific outcomes and

prior radiation exposure are necessarily expressed in terms of probability using estimates
of risk derived from epidemiologic studies of irradiated populations, and taking into
account known risk factors such as age at exposure and gender.
3.3.1

Heritable Genetic Effects

There is no genetic disease that is uniquely radiogenic. Increased rates of conditions
associated with inherited genetic mutations have been observed amongthe progeny of
experimentally irradiated organisms. However, to date there is no evidence ofstatistically
significant increases in the rates of genetic diseases or conditions among the progeny of
irradiated populations (30).
3.3.2

Somatic Effects

Epidemiologic studies of such populations have clearly identified the major stochastic
effect of ionizing radiation to be a dose-related increase in the risk of tumors, primarily
malignant tumors. This association has been demonstrated statistically for all cancers
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