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Table 1 Characteristics of study participants with 3q29Del and controls

From: Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry

 

3q29 deletion syndrome

Control

p value

Age, years (mean ± SD)

10.0 ± 8.6

9.9 ± 7.2

0.945

Sex (n, %)

  

0.521

 Male

54 (58.1%)

33 (51.6%)

 

 Female

39 (41.9%)

31 (48.4%)

 

Race (n, %)

  

0.0003

 White

81 (87.1%)

41 (64.1%)

 

 Black/African American

2 (2.2%)

12 (18.8%)

 

 Other

10 (10.8%)

9 (14.1%)

 

 Blank

0 (0%)

2 (3.1%)

 

Heart defect (n, %)

  

2.37E− 07

 Yes

27 (29.0%)

2 (3.1%)

 

 No

54 (58.1%)

61 (95.3%)

 

 Blank

12 (12.9%)

1 (1.6%)

 

Age at walking (n, %)

  

2.16E− 09

 Normal

42 (45.7%)

60 (93.8%)

 

 Delayed

23 (25.0%)

1 (1.6%)

 

 Extremely delayed

12 (13.0%)

1 (1.6%)

 

 Unsure

10 (10.9%)

2 (3.1%)

 

 Not applicable

5 (5.4%)

0 (0%)

 
  1. Demographic data collected from the custom medical and demographic questionnaire completed by participants upon enrollment in the online 3q29 Registry. p values were calculated with Student’s t test (age), Fisher’s exact test (race, heart defect, age at walking), or Pearson’s chi square test (sex)
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Molecular Autism

ISSN: 2040-2392