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. 2017 Sep 15;17:182. doi: 10.1186/s12883-017-0959-2

Table 1.

Familial cases presenting with distinct clinical phenotypes

Case Age onset; number of patients First symptom Phenotype Brain atrophy Ethnic origin GRN mutation
Rovelet-Lecrux et al., 2008 [15] 67,77; 2 patients Language dysfunction PPA left > right French g.95_4390del
Resting tremor PD
Spina et al., 2007 [13] 45,73; 2 patients Involuntary arm movement CBS right > left N/A g.26C >A
Cognitive decline AD
Beck et al., 2008 [4] 54–67; 10 patients Language dysfunction PPA left > right (n = 2) United Kingdom g.90_91insCTGC
Limb apraxia CBS right > left (n = 1)
Skoglund et al., 2009 [12] 46–59; 10 patients Language dysfunction PPA N/A Swedish g.102delC
Limb apraxia CBS
Rademakers et al., 2007 [16] 62,66; 2 patients N/A FTLD, CBS N/A American g.3240C > T
Masellis et al., 2006 [17] 57,62; 2 patients Behavioral changes FTLD right > left Canadian family of Chinese origin g.1637G > A
Axial and extremity rigidity CBS
Leverenz et al., 2007 [18] 35–69; 9 patients Language dysfunction FTLD left > right (n = 3)
right > left (n = 1)
American g.1871A > G
Anxiety, apathy PPA
Parkinsonism PD
López de Munain et al., 2008 [19] 53,57; 2 patients N/A FTLD, CBS N/A Basque Country g.1872G > A
51,71; 2 patients N/A FTLD, CBS N/A Basque Country g.1873G > A
65; 2 patients N/A FTLD, CBS N/A Basque Country g.1874G > A
60; 2 patients N/A FTLD, CBS N/A Basque Country g.1875G > A
63–70; 4 patients N/A FTLD, CBS N/A Basque Country g.1876G > A
52; 2 patients N/A FTLD, ALS N/A Basque Country g.1877G > A
Benussi et al., 2009 [5] 60–71; 5 patients Language dysfunction PPA right > left Italian g.1977_1980delCACT
Parkinsonism CBS
Kelley et al., 2009 [6] N/A; 6 patients N/A FTLD, PD symmetrical American g.2273_2274insTG
N/A; 6 patients N/A FTLD, PD right > left American g.2597delC
Pietroboni et al., 2011 [7] 47–79; 5 patients Memory impairment, Acalculia FTLD, AD right > left (n = 1)
symmetrical (n = 1)
N/A (n = 3)
Italian g.63_64insC
Language impairment
Rossi et al., 2011 [8] 47–80; 6 patients Behavioural abnormality FTLD
Dementia
Left > right Italian g.1761_1762delCA
Language dysfunction
Attention impairment
The present case 75,62; 2 patients Language dysfunction PPA left > right Japanese g.1118_1119delCCinsG
Limb apraxia CBS

AD Alzheimer’s disease, ALS amyotrophic lateral sclerosis, CBS corticobasal syndrome, FTLD frontotemporal lobar degeneration, GRN progranulin gene, N/A not available, PD Parkinson’s disease, PPA primary progressive aphasia