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Table 1 Selected clinical, neuropathological and genetic details on patients studied. FTLD = Frontotemporal Lobar degeneration; MND = Motor Neurone Disease

From: Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 gene

Group

M/F

Age at onset (y)

Age at death (y)

Duration of illness (y)

FTLD-TDP type A (n = 25)

14/11

61.0 ± 5.9

69.0 ± 5.1

8.0 ± 3.3

FTLD-TDP type B (n = 15)

9/6

57.1 ± 7.4

62.3 ± 8.0

5.3 ± 4.5

FTLD-TDP type C (n = 10)

6/4

59.9 ± 7.1

71.8 ± 5.7

11.9 ± 5.0

FTLD-tau (n = 11)

4/7

51.4 ± 6.4

61.4 ± 5.4

10.0 ± 3.1

MND (n = 4)

4/0

53.3 ± 7.3

56.3 ± 8.3

3.0 ± 1.4

FTLD/MND C9orf72 expansion (n = 21)

13/8

57.3 ± 6.0

63.5 ± 6.4

6.2 ± 4.1

FTLD GRN mutation (n = 9)

5/4

60.7 ± 5.6

69.3 ± 4.1

8.7 ± 3.9

FTLD No mutation (n = 24)

15/9

60.2 ± 7.8

68.5 ± 8.9

8.4 ± 4.9

FTLD MAPT mutation (n = 11)

4/7

51.4 ± 6.4

61.4 ± 5.4

10.0 ± 3.1

Healthy Controls (n = 10)

3/7

na

83.3 ± 7.6

na