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Information Journal Paper

Title

A CASE OF AUTISTIC BOY WITH HETEROMORPHISM OF MATERNAL NUMBER 15 CHROMOSOME

Pages

  322-329

Abstract

 Introduction: Infantile autism is a clinical heterogenous disorder with unknown etiology. Evidences from the relatively few family and twin studies suggest a genetic component. It is concluded that in some cases chromosomal rearrangements are the basic causes. The aim of the present work is to report a 4-year-old autistic boy with a genetic approch. Materials & Methods: Family history, pedigree pattern and chromosomes of the proband and his parents were studied (G-banding). Results: There was no any other case in his family history. Chromosomal study has revealed a maternal origin rearranged chromosome number 15. Conclusion: The results of present study confirmed that chromosomal study is one of the first necessities in the study of autism, and it will help us for a better genetic counseling with families with an autisic child.

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    APA: Copy

    POURJAFARI, H., & HASHEMZADEH CHALESHTORI, M.. (2003). A CASE OF AUTISTIC BOY WITH HETEROMORPHISM OF MATERNAL NUMBER 15 CHROMOSOME. STUDIES IN MEDICAL SCIENCE (THE JOURNAL OF URMIA UNIVERSITY OF MEDICAL SCINCES), 13(4), 322-329. SID. https://sid.ir/paper/63649/en

    Vancouver: Copy

    POURJAFARI H., HASHEMZADEH CHALESHTORI M.. A CASE OF AUTISTIC BOY WITH HETEROMORPHISM OF MATERNAL NUMBER 15 CHROMOSOME. STUDIES IN MEDICAL SCIENCE (THE JOURNAL OF URMIA UNIVERSITY OF MEDICAL SCINCES)[Internet]. 2003;13(4):322-329. Available from: https://sid.ir/paper/63649/en

    IEEE: Copy

    H. POURJAFARI, and M. HASHEMZADEH CHALESHTORI, “A CASE OF AUTISTIC BOY WITH HETEROMORPHISM OF MATERNAL NUMBER 15 CHROMOSOME,” STUDIES IN MEDICAL SCIENCE (THE JOURNAL OF URMIA UNIVERSITY OF MEDICAL SCINCES), vol. 13, no. 4, pp. 322–329, 2003, [Online]. Available: https://sid.ir/paper/63649/en

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