Esra Çöp, Pinar Yurtbaşi, Özgür Öner, Kerim M Münir
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Genetic testing in children with autism spectrum disorders.
Objective: The aim of this study was to investigate karyotype abnormalities, MECP2 mutations, and Fragile X in a clinical population of children with Autism Spectrum Disorders (ASD) using The Clinical Report published by the American Academy of Pediatrics.
Methods: Ninety-six children with ASD were evaluated for genetic testing and factors associated with this testing.
Results: Abnormalities were found on karyotype in 9.7% and in DNA for fragile X in 1.4%. Karyotype abnormalities include inv(9)(p12q13); inv(9)(p11q13); inv(Y)(p11q11); Robertsonian translocation (13;14)(8q10q10) and (13,14)(q10q10); 9qh+; Yqh+; 15ps+; deletion 13(p11.2).
Conclusion: Genetic testing should be offered to all families of a child with an ASD, even not all of them would follow this recommendation. Although karyotype and FRAXA assessment will yield almost 10% positive results, a detailed history and physical examination are still the most important aspect of the etiological evaluation for children with ASD. Also, it is important to have geneticists to help in interpreting the information obtained from genetic testing.
期刊介绍：
The aim of Anatolian Journal of Psychiatry (Anadolu Psikiyatri Dergisi) is to present on a scientific level and share the theoretical information and clinical experience in the field of behavioral sciences, primarily psychiatry, and create a forum. Anatolian Journal of Psychiatry aims to reach a national and international audience and will accept submissions from authors worldwide. It gives high priority to original studies of interest to clinicians and scientists in social psychiatry and related disciplines. Anatolian Journal of Psychiatry publishes high quality research targeted to specialists, residents and scientists in psychiatry, psychology, neurology, pharmacology, applied and basic neurosciences, genetics, physiology, psychiatric nursing, and related sciences.
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