Table 1 Demographic and phenotypic characteristics of the sample.

From: Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use

 

% (N/253)

Males

81.4% (206)

Family history

27.7% (70)

Consanguinity

1.6 % (4)

Asperger syndrome

35.6% (90)

Intellectual disability

26.9% (68)

Dysmorphic features

26.5% (67)

Premature birth

3.95% (10)

Microcephaly

3.7% (9)

Macrocephaly

7.9% (20)

Epilepsy

7.1% (18)

Back to article page