Table 2. Clinical and molecular features of heterozygous (MV) iCJD cases analyzed.
Case ID Number | Gender | Age at Onset a | Duration b | Molecular Sub-classification | Brain Region c | PrPSc Type d | M129 (%) e |
---|---|---|---|---|---|---|---|
15 | M | 33 | 8 | iCJD MV2 | CC | 2d | 39 ± 9 |
16 | F | 30 | 12 | iCJD MV2 | CC | 2d | 38 ± 14 |
17 | M | 32 | 16 | iCJD MV2 | CC | 2+1 | 46 ± 3 |
18 | M | 28 | 16 | iCJD MV2 | CC | 2d | 36 ± 5 |
19 | F | 27 | 32 | iCJD MV2 | CC | 2d | 66 ± 4 |
20 | F | 32 | 23 | iCJD MV2 | CC | 2+1 | 39 ± 6 |
aAge of onset in years.
bDisease duration in months.
cCC = cerebral cortex.
dPrPSc typing according to the method of Parchi et al. [33].
eMean percentage ± SD of PrPSc with M129.
There was no significant correlation of percentage PrPSc-M129 with iCJD type, age of onset, or disease duration (p>0.3).