Table 1 Demographics of 13 participants with pediatric genetic white matter disorders
From: Genotypic and phenotypic heterogeneity among Chinese pediatric genetic white matter disorders
Participants (n = 13) | |
|---|---|
Male/Female n(%) | 11 (84.6%) / 2 (15.4%) |
Age (years old) | 17.0 ± 9.7 |
Age of onset (years old) | 10.0 ± 5.5 |
Family history (+/-) n(%) | 1 (7.7%) / 12 (92.3%) |
Motor disorder (+/-) n(%) | 9 (69.2%) / 4 (30.8%) |
Cognitive impairment (+/-) n(%) | 11 (84.6%) / 2 (15.4%) |
Behavioral abnormality (+/-) n(%) | 2 (15.4%) / 11 (84.6%) |
Seizure (+/-) n(%) | 2 (15.4%) / 11 (84.6%) |
Dysuria (+/-) n(%) | 3 (23.1%) / 10 (76.9%) |
Visual impairment (+/-) n(%) | 4 (30.8%) / 9 (69.2%) |
Auditory impairment (+/-) n(%) | 2 (15.4%) / 11 (84.6%) |
APOE-ε4 (+/-) n(%) | 1 (7.7%) / 12 (92.3%) |
Causative mutation (+/-) n(%) | 11 (84.6%) / 2 (15.4%) |