Statements (56)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:neurodegenerative_diseases
|
| gptkbp:affects |
gptkb:language
behavior personality |
| gptkbp:can_lead_to |
increased caregiver burden
loss of independence |
| gptkbp:caused_by |
degeneration of the frontal and temporal lobes
|
| gptkbp:diagnosis |
clinical assessment
neuroimaging progressive decline average survival of 6 to 12 years after diagnosis |
| https://www.w3.org/2000/01/rdf-schema#label |
frontotemporal dementia
|
| gptkbp:is |
gptkb:normal_pressure_hydrocephalus
gptkb:neurodegenerative_diseases vascular dementia |
| gptkbp:is_associated_with |
TDP-43 protein abnormalities
tau protein abnormalities |
| gptkbp:is_characterized_by |
behavioral changes
early onset executive dysfunction language difficulties |
| gptkbp:is_common_in |
younger adults
people aged 40 to 65 |
| gptkbp:is_considered_as |
a challenging diagnosis
a rare form of dementia a significant public health issue |
| gptkbp:is_discussed_in |
research studies
support groups medical conferences |
| gptkbp:is_documented_in |
gptkb:literature
gptkb:guidelines |
| gptkbp:is_influenced_by |
environmental factors
genetic factors |
| gptkbp:is_managed_by |
gptkb:psychology
social workers neurologists multidisciplinary team |
| gptkbp:is_part_of |
gptkb:neurodegenerative_diseases
cognitive disorders |
| gptkbp:is_recognized_by |
genetic testing
family history |
| gptkbp:is_related_to |
gptkb:Pick's_disease
gptkb:neurodegenerative_diseases motor neuron disease |
| gptkbp:is_studied_in |
neurology
psychiatry |
| gptkbp:symptoms |
difficulty in speaking
apathy compulsive behavior changes in social behavior loss of empathy |
| gptkbp:treatment |
supportive care
medications for symptoms |
| gptkbp:bfsParent |
gptkb:amyotrophic_lateral_sclerosis
gptkb:neurodegenerative_diseases |
| gptkbp:bfsLayer |
4
|