Frontotemporal Degeneration (FTD) is a neurodegenerative disorder affecting the frontal and temporal lobes of the brain. The ICD-10 code for FTD is G31.09, which falls under the category of "Other specified degenerative diseases of nervous system." In the previous coding system, ICD-9, FTD was classified under code 331.19, which represented "Other specified cerebral degenerations."
Frontotemporal degeneration (FTD) is a neurodegenerative disorder that affects the frontal and temporal lobes of the brain. It is characterized by progressive changes in behavior, language, and personality. In the International Classification of Diseases, 10th Revision (ICD-10), FTD is classified under the code G31.0. This code specifically refers to "Frontotemporal dementia" which encompasses the various subtypes of FTD.
In contrast, the International Classification of Diseases, 9th Revision (ICD-9) does not have a specific code for FTD. Instead, it falls under the broader category of "Other degenerative diseases of the nervous system" with code 331.9. However, it is important to note that ICD-9 codes are no longer in use as they have been replaced by ICD-10 codes since October 1, 2015.
FTD is a complex condition that presents with a range of symptoms, making its diagnosis challenging. Common symptoms include changes in personality and social behavior, language difficulties, impaired judgment, and executive function deficits. As the disease progresses, individuals may experience memory problems, muscle weakness, and difficulties with movement control.
Early detection and accurate diagnosis of FTD are crucial for appropriate management and support. Medical professionals utilize various diagnostic criteria and assessments to differentiate FTD from other neurodegenerative disorders, such as Alzheimer's disease. Prompt identification allows for the implementation of tailored treatment plans and support services to enhance the quality of life for individuals with FTD and their caregivers.