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Table 4 Demographic data

From: Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family

Patient

Sex

FH

AO (years)

Age of death (years)

DD (years)

Final clinical diagnosis

DR2.3

F

F - autosomal dominant

63

72

8.6

PPA (NFV)

DR8.1

F

F - autosomal dominant

62

68

5.9

bvFTD

DR25.1

F

F - autosomal dominant

69

75

5.4

bvFTD

DR25.5

M

F - autosomal dominant

70

73

3,4

bvFTD

DR28.1

M

F - autosomal dominant

56

62

6.8

PPA (NFV)

DR205.1

F

F

55

61

5.1

PD

DR31.1

M

F

65

70

5.6

PPA (NFV)

DR1207.1

F

S

62

66

4.4

PPA (NFV)

DR1213.1

M

F - autosomal dominant

58

60

2.3

bvFTD

  1. Abbreviations: FH Familial history), F Familial presentation, S Sporadic, AO Age of onset, DD Disease duration in years, PPA Primary progressive aphasia, NFV Nonfluent variant, bvFTD Behavioral variant frontotemporal dementia