The goal of the Family Genetic Study is to uncover the genetic and non-genetic factors important in the development of Tourette Syndrome (TS), Attention Deficit Hyperactivity Disorder (ADHD), and Obsessive Compulsive Disorder (OCD). The main purpose of this work is to collect information about behavioral patterns that are shared in common by these disorders. We will also look at whether those behavioral patterns are inherited. This study is funded by the National Institute for Neurological Disorders and Stroke (NINDS).
Who is eligible to participate in this research? We are looking for families with at least one child age 6 or older who is diagnosed with TS, OCD, and/or ADHD.
Studies Our research studies are aimed at developing a better understanding of neurobiological changes that underlie OCD, understanding ways in which different forms of OCD may be distinct from one another, and development of novel pharmacological treatments.
All patients who come to us receive a thorough and thoughtful clinical evaluation by Clinic psychiatrists and other personnel. We will seek to understand your condition, what treatments you have tried in the past (and which have benefited you), and any other issues – psychiatric, medical, or social – that may be affecting your symptoms and quality of life. In many cases, and in all cases where participation in one of our research studies seems appropriate, this evaluation will also involve a physical examination, laboratory tests, and an electrocardiogram. Some patients do not seem a good match for our research studies, in which case we endeavor to provide a useful treatment consultation; in some cases we are able to offer ongoing medication management or psychotherapy. If participation in one of our studies seems appropriate, those options will be thoroughly explained to you so that you can make an informed decision as to which research you wish to participate in.
