Objective: To determine whether siblings with pervasive developmental disor
ders (PDD) tend to have the same type and number of PDD symptoms or a simil
ar level of functioning. Method: The familiar correlations for PDD subtype,
symptom totals, adaptive behaviors, and nonverbal IQ were calculated for 9
4 children with PDD from 46 families. Results: On variables measuring PDD s
ymptoms, only impairments in nonverbal communication and verbal/nonverbal s
tatus tended to run true within families. There was no familial aggregation
of PDD subtype. In contrast, measures of nonverbal IQ and adaptive behavio
rs in socialization and communication showed a moderate degree of familial
resemblance. The degree of familial resemblance did not change ii the analy
sis was restricted only to those families in which both affected children m
et criteria for autism. Conclusion: Insofar as the familial resemblance see
n in PDD is due to genetic factors, these data provide some evidence that h
igher- and lower-functioning PDD children may arise from separate genetic m
echanisms. Current gene-mapping studies of PDD may need to take this eviden
ce of genetic heterogeneity into account.