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Obsessive–Compulsive Disorder

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Abstract

Obsessive–compulsive disorder (OCD) is the fourth most common neuropsychiatric disorder, with lifetime prevalence estimates of 0.4 to 3.5%. Family and twin studies suggest a strong genetic component, and molecular genetic studies are being carried out to identify genes contributing risk to OCD. OCD is postulated as a frontal–striatal disorder, and functional neuroimaging studies provide a strong support for the dysfunction of the cortico–striatal–thalamic–cortical neurocircuit. OCD can be secondary to a variety of medical conditions, which range from deteriorative neurological illness, to head injury, and to autoimmune disorders. Few reports and no controlled studies exist in the treatment of acquired/secondary OCD. Both cognitive–behavioral therapy (CBT) and pharmacotherapy are effective first-line treatment modalities for OCD. Brain stimulation and/or psychosurgery have been tried with varying success in treatment of refractory OCD. Environmental, genetic, and clinical factors interact in a complex fashion in the individual patient. This chapter examines OCD from the medical perspective.

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Murphy, T.K., Frazier, S., Kim, SJ. (2008). Obsessive–Compulsive Disorder. In: Fatemi, S.H., Clayton, P.J. (eds) The Medical Basis of Psychiatry. Humana Press. https://doi.org/10.1007/978-1-59745-252-6_10

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