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. 2024 Oct 3;14(5):161–172. doi: 10.1080/17582024.2024.2404378

Table 2.

Characteristics of genetic survey respondents.

Characteristic Totala
Personally diagnosed with ALSP, n/N (%) 22/58 (37.9)
Number of family members (including the survey respondent) who experienced ALSP symptoms n/N (%)  
 1 10/50 (20.0)
 2 12/50 (24.0)
 3 20/50 (40.0)
 4 1/50 (2.0)
 5 or more 7/50 (14.0)
  Had genetic testing Did not have genetic testing Total
Respondent age group (years), n/N (%)
 18–25 2/30 (6.7) 2/20 (10.0) 4/58 (6.99)
 26–35 4/30 (13.3) 6/20 (30.0) 10/5858 (17.22)
 36–45 5/30 (16.7) 6/20 (30.0) 13/58 (22.44)
 46–55 11/30 (3.7) 3/20 (15.0) 18/58 (31.00)
 56–65 5/30 (16.7) 3/20 (15.0) 10/58 (17.22)
 66–75 2/30 (6.7) 0 2/58 (3.4)
 76 or older 1/30 (3.3) 0 1/58 (1.7)
a

Fifty-eight surveys with qualifying responses were received, and surveys with complete results were received from 39 respondents.

ALSP: Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia.