有人认为，染色体异常可能会占孤独症病例的百分之十到二十，而15q11-13区段的染色体重复，是目前唯一所知的能和孤独症相关联的异常。
Chromosomal abnormalities are thought to account for 10 to 20 percent of cases and duplication of chromosome 15q11-13 is the only recurrent aberration so far linked to the disease.
有人认为，染色体异常可能会占孤独症病例的百分之十到二十，而15q11-13区段的染色体重复，是目前唯一所知的能和孤独症相关联的异常。
Chromosomal abnormalities are thought to account for 10 to 20 percent of cases and duplication of chromosome 15q11-13 is the only recurrent aberration so far linked to the disease.
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