A government report addressing concerns about the many implications of prenatal and newborn genetic testing outlined policy guidelines and legislative recommendations intended to avoid involuntary and
ineffective testing and to protect confidentiality. The report recommended that all such screening be voluntary.
Citing results of two different voluntary newborn screening programs, the report said these programs can achieve compliance rates equal to or better than those of mandatory programs. State health departments
might be wise to eventually mandate the offering of tests for diagnosing treatable conditions in newborns;
however, careful pilot studies for conditions diagnosable at birth need to be done first. Although the report asserted that it would prefer that all screening be voluntary, it did note that if a state elects to mandate newborn screening for a particular condition, the state should do so only if there is strong evidence that a newborn would benefit from effective treatment at the earliest possible age.Newborn screening is the most common type of genetic screening today. More than four million newborns are tested annually so that effective treatment can be started in a few hundred infants. Obtaining informed consenta process that would include educating participants, not just processing documentswould enhance voluntary participation.
When offered testing, parents should receive comprehensive counseling, which should be nondirective.
Relevant medical advice, however, is recommended for treatable or preventable conditions.
On the basis of above passage please answer the following question Based on the passage, for which of the following would the government report LEAST likely recommend mandated genetic testing?