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Table 2 Demographic and clinical characteristics of persons with AS

From: The economic impact of caregiving for individuals with Angelman syndrome in the United States: results from a caregiver survey

Demographic variables

N = 105

Age in years, n (%)

   0 to 5

32 (30.5%)

   6 to 12

40 (38.1%)

   13 to 17

15 (14.3%)

   18+

18 (17.1%)

Sex (male), n (%)

52 (49.5%)

Race, n (%)

   Asian

8 (7.6%)

   Black or African American

5 (4.8%)

   Hispanic or Latino

14 (13.3%)

   Native Hawaiian or other Pacific Islander

1 (1.0%)

   White

90 (85.7%)

Clinical and caregiving-related variables

AS genotype, n (%)

   Deletion

51 (48.6%)

   Mutation

26 (24.8%)

   Imprinting center defect

2 (1.9%)

   Uniparental disomy

6 (5.7%)

   Mosaic

1 (1.0%)

   Unknown/not reported

19 (18.1%)

Ability for person with AS to be left alone, n (%)

   No, she/he needs continuous surveillance

101 (96.2%)

   Yes, for less than one hour

4 (3.8%)

   Yes, she/he can easily be left along for several hours (or more)

0 (0.0%)

  1. AS Angelman syndrome