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Introduction: Frontotemporal dementia (FTD) was first described in 1892 and consists of a frontotemporal atrophy that preserves the posterior lobes. Genetically, several changes have been associated with the disease. Its clinical manifestation occurs through three presentations, such as: behavioral variant, non-fluent variants and semantics. The diagnosis relies on magnetic resonance imaging to rule out other diseases. Treatment is through the use of Serotonin Reuptake Inhibitors (SSRIs) to improve behavioral symptoms, including Behavioral changes to frontotemporal dementia diagnosis