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. 2024 Nov 6;148(1):60. doi: 10.1007/s00401-024-02807-w

Table 1.

Cases by primary neuropathological diagnosis

Diagnosis Total Birth sex Age at death Biondi bodies
Female Male N/A Mean Min Max N/A  + 
Alzheimer disease, Dominantly Inherited 27 14 13 0 51.2 34 76 1 15 12
Alzheimer disease, Sporadic 439 238 198 3 77.4 40 103 3 423 16
Diffuse Lewy body disease 139 41 98 0 78.5 58 95 0 137 2
Multiple system atrophy 6 4 2 0 71.5 52 83 0 6 0
FTLD-Tau, Hereditary 18 9 9 0 58.2 47 65 0 14 4
FTLD-Tau, Sporadic 78 34 44 0 72.3 49 94 0 74 4
FTLD-TDP-43, Hereditary 38 16 22 0 64.3 42 81 0 35 3
FTLD-TDP-43, Sporadic 23 9 14 0 68.1 50 92 0 20 3
Creutzfeldt-Jakob disease, Hereditary 9 5 4 0 61.7 42 85 0 7 2
Creutzfeldt-Jakob disease, Sporadic 115 65 50 0 65.3 33 91 0 93 22
Gerstmann-Sträussler-Scheinker disease 30 12 17 1 53.9 38 73 1 15 15
Amyotrophic lateral sclerosis 14 4 10 0 64.6 49 77 0 14 0
Cerebrovascular disease 27 9 18 0 80.3 52 98 0 26 1
Miscellaneous 29 11 18 0 55.5 5 85 1 18 11
To be determined 134 45 74 15 66.3 14 96 18 108 26
TOTAL 1126 516 591 19 71.73 5 103 24 1005 121

Frontotemporal Lobar Degeneration (FTLD), TAR DNA-binding protein 43 (TDP-43), Positive ( +), Negative (−)