Section 63-6-803 - Scope of genetic counselingGenetic counseling is a communication process, conducted by one (1) or more appropriately trained individuals, that includes:
(1) Estimating the likelihood of occurrence or recurrence of any potentially inherited or genetically influenced condition. This assessment may involve:(A) Obtaining and analyzing a complete health history of the person and family;(B) Reviewing pertinent medical records;(C) Evaluating the risks from exposure to possible mutagens or teratogens; and(D) Recommending genetic testing or other evaluations to assist in the diagnosis of a condition or determine the carrier status of one (1) or more family members;(2) Helping the individual, family, health care provider or public to:(A) Appreciate the medical, psychological and social implications of a disorder, including its features, variability, usual course and management options;(B) Learn how genetic factors contribute to the disorder and affect the chance for recurrence of the condition in other family members;(C) Understand available options for coping with, preventing, or reducing the chance of occurrence or recurrence of a condition;(D) Select the most appropriate, accurate and cost-effective methods of diagnosis; and(E) Understand genetic tests, including, but not limited to, diagnostic genetic tests, screening tests or predispositional genetic tests, coordinate testing for inherited disorders and interpret complex genetic test results;(3) Facilitating an individual's or family's: (A) Exploration of the perception of risk and burden associated with a genetic disorder;(B) Decision making regarding testing or medical interventions consistent with their beliefs, goals, needs, resources, culture and ethical/moral views; and(C) Adjustment and adaptation to the condition or their genetic risk by addressing needs for psychological, social and medical support. Acts 2007 , ch. 366, § 1.