Complex autism spectrum disorder in a patient with a 17q12 microduplication

Autism spectrum disorders (ASDs) are phenotypically complex developmental neuropsychiatric disorders affecting approximately 0.6% of the population. About 30–70% of affected children are also considered to have intellectual disability (ID). The underlying genetic causes of ASDs are diverse with a de...

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Bibliographic Details
Published in:	American journal of medical genetics. Part A Vol. 158A; no. 5; pp. 1170 - 1177
Main Authors:	Brandt, Tracy, Desai, Khyati, Grodberg, David, Mehta, Lakshmi, Cohen, Ninette, Tryfon, Ana, Kolevzon, Alexander, Soorya, Latha, Buxbaum, Joseph D., Edelmann, Lisa
Format:	Journal Article
Language:	English
Published:	Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-05-2012 Wiley-Liss Wiley Subscription Services, Inc
Subjects:	17q12 microduplication array CGH autism Biological and medical sciences Child clinical studies Child Development Disorders, Pervasive - genetics Child, Preschool Chromosome Deletion Chromosome Duplication Chromosomes, Human, Pair 17 Comparative Genomic Hybridization Developmental disorders Humans Infantile autism Intellectual Disability - genetics Male Medical genetics Medical sciences Parents Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry recurrent rearrangement Human Nervous system diseases Relapse array CGH 17q12 microduplication Patient Developmental disorder Recurrent Complexes recurrent rearrangement Autism Pervasive developmental disorder Neurological disorder
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