Table 2.
Data provided by respective Brain Bank corresponding to patients affected by each CJD type.
| Patient | Aetiology | Gender | Age | Genetic Data | PrP Isotype |
|---|---|---|---|---|---|
| 1 | Sporadic | M | 70 | MM nil | 2 |
| 2 | Sporadic | M | 70 | MM nil | 2 |
| 3 | Sporadic | F | 78 | MM nil | 1 |
| 4 | Sporadic | M | 71 | MV nil | 2 |
| 5 | Sporadic | F | 63 | MV nil | 2 |
| 6 | Sporadic | F | 71 | MV nil | 2 |
| 7 | Sporadic | M | 74 | VV nil | 2 |
| 8 | Sporadic | F | 73 | VV nil | 2 |
| 9 | Sporadic | F | 77 | VV nil | 2 |
| 10 | Familial | F | 56 | MM E200K | na |
| 11 | Familial | M | 78 | MV E200K | na |
| 12 | Familial | F | 53 | MM E200K | na |
| 13 | Iatrogenic (GHT) | M | 42 | MM nil | 1 |
| 14 | Iatrogenic (GHT) | F | 34 | MV nil | 1 + 2 |
| 15 | Iatrogenic (DURA) | F | 27 | MM nil | 1 |
| 16 | Variant | M | 59 | MM nil | 2B |
| 17 | Variant | M | 62 | MM nil | 2B |
| 18 | Variant | F | 32 | MM nil | 2B |
| 19 | VPSPr | M | 66 | VV | |
| 20 | VPSPr | F | 76 | VV lMWt | |
| 21 | VPSPr | M | 66 | MV | |
| 22 | Control | F | 69 | ||
| 23 | Control | M | 63 | ||
| 24 | Control | M | 74 |
PrP, prion protein; na, not available data; MM, MV, VV (M, methionine; V, valine): genotypes at codon 129 of PrP gene; Mutations are indicated when PrP gene mutation present; Nil, when no present.