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Asperger Syndrome: Familial and Pre- and Perinatal Factors

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Publisher Springer
Date 2005 May 25
PMID 15909402
Citations 17
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Abstract

Objective: Study familial and pre- and perinatal factors in Asperger Syndrome (AS).

Methods: One hundred boys with AS had their records reviewed. "Pathogenetic subgroups" were defined according to presence of medical syndromes/chromosomal abnormalities, indices of familiality, and pre- and perinatal risk factors predisposing to brain damage.

Results: No major index of pathogenetic factors was found in 13%, a syndrome/chromosomal abnormality in 8%, pre- or perinatal risk 13%, combined pre- or perinatal risk and family history in 11%, and family history only in 55%.

Comment: About 50% of all boys with AS have a paternal family history of autism spectrum disorder. Pre- and perinatal risks appear to be important in about 25% of cases.

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References
1.
Delong R, Nohria C . Psychiatric family history and neurological disease in autistic spectrum disorders. Dev Med Child Neurol. 1994; 36(5):441-8. View

2.
Mesibov G, Schopler E, Schaffer B, Michal N . Use of the childhood autism rating scale with autistic adolescents and adults. J Am Acad Child Adolesc Psychiatry. 1989; 28(4):538-41. DOI: 10.1097/00004583-198907000-00012. View

3.
Ehlers S, Gillberg C . The epidemiology of Asperger syndrome. A total population study. J Child Psychol Psychiatry. 1993; 34(8):1327-50. DOI: 10.1111/j.1469-7610.1993.tb02094.x. View

4.
Debeer P, Peeters H, Driess S, De Smet L, Freese K, Matthijs G . Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations. Am J Med Genet A. 2003; 120A(1):49-58. DOI: 10.1002/ajmg.a.20018. View

5.
Briskman J, Happe F, Frith U . Exploring the cognitive phenotype of autism: weak "central coherence" in parents and siblings of children with autism: II. Real-life skills and preferences. J Child Psychol Psychiatry. 2001; 42(3):309-16. View