Abstract

Frontotemporal dementia (FTD) is a progressive neurodegenerative disorder that predominantly affects individuals at an early age, typically between 40 and 65 years. Characterized by changes in behavior, personality, and language, FTD is often misdiagnosed as psychiatric illness due to its early behavioral manifestations. This study explores the clinical features of FTD and the significant impact it has on patients and their families. We examine the range of symptoms, including executive dysfunction, disinhibition, and aphasia, along with how they manifest in early-onset cases. Additionally, we assess the emotional, psychological, and financial burdens placed on family members and caregivers. The study aims to provide insights into the challenges faced by individuals diagnosed with FTD and their families, ultimately contributing to a more comprehensive understanding of early-onset neurodegeneration. By recognizing these features early, proper interventions can be implemented to help manage symptoms and improve quality of life for both patients and caregivers.