Table 1.
Case 1 * | Case 2 * | Case 3 | ||
---|---|---|---|---|
Autopsy | Autopsy | Stereotactic biopsy | ||
Age at onset (years) | 37 | 44 | 39 | |
Sex | Female | Male | Female | |
Duration of disease | 4 years | 10 years | 3 years | |
Cognitive impairment | Present | Present | Present | |
Psychiatric symptoms (e.g., depression, apathy, abulia, indifference, anxiety, irritability, distraction) | Present | Present | Present | |
Pyramidal signs (hyperreflexia, spasticity, increased tone in extremities, pseudobulbar palsy) | Present | Present | Present | |
Parkinsonism (resting tremor, rigidity, bradykinesia, postural instability) | Present | Present | Present | |
Epilepsy | Absent | Present (at advanced stage) | Absent | |
Autosomal dominant (AD) inheritance or sporadic occurrence | AD | AD | Sporadic | |
Bilateral cerebral white matter lesions | Present | Present | Present | |
Thinning of the corpus callosum | Present | Present | Present | |
Stage (by Oyanagi) | II | III | N/A | |
CSF1R mutation (pathogenic variant) | c.2345G > A | c.2345G > A | c.1765G > A |
* Cases 1 and 2 occurred in siblings.