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. 2020 Jan;41(1):160–166. doi: 10.3174/ajnr.A6324

Table 1:

Baseline clinical and demographic characteristics

Total Sample (n = 37)
Demographic characteristics
Female (No.) (%) 21 (56.8)
Age at moyamoya diagnosis (median) (IQR, 25–75) (yr) 10 (6.3–11.8)
Age at initial CVR (median) (IQR, 25–75) (yr) 10.7 (7.5–14.7)
Time to follow-up (median) (IQR, 25–75) (mo) 20.8 (13.7–84.1)
Moyamoya classification
 Idiopathic 14 (37.8)
 Syndromic 23 (62.2)
  NF1 9 (24.3)
  Trisomy 21/other chromosomal disorders 7 (18.9)
  Sickle cell disease 5 (13.5)
  Postradiation vasculopathy 2 (5.4)
Clinical presentation
 Stroke (No.) (%) 12 (32.4)
  Bilateral 2 (5.4)
  Right 6 (16.2)
  Left 4 (10.8)
 TIA (No.) (%) 8 (21.6)
 Seizure (No.) (%) 3 (8)
 Headaches (No.) (%) 8 (21.6)
 Asymptomatic (No.) (%) 6 (16.2)
 Other (No.) (%) 2 (5.4)
Radiographic findings (No.) (%)
 Parenchymal
  Not ischemic 8 (21.6)
  Watershed 12 (32.4)
   Deep white matter 1 (2.7)
   Cortical 12 (32.4)
 Cortical 3 (8.1)
 Cortical ischemic and watershed 14 (37.8)
 Vascular
  Moyamoya laterality (No.) (%)
   Left 8 (21.6)
   Right 6 (16.2)
   Bilateral 23 (62.2)
 Grade of stenosis (No.) (%)
 50%–74% Occlusion 5 (13.5)
 ≥75% Occlusion 32 (86.5)

Note:—NF1 indicates neurofibromatosis type 1.