Genetic Counseling for Families with Sporadic Intellectual Disability in North of Iran: A Retrospective Study

سال انتشار: 1399
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 136

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شناسه ملی سند علمی:

JR_INJPM-8-8_006

تاریخ نمایه سازی: 5 شهریور 1402

چکیده مقاله:

Background Intellectual Disability (ID) is a heterogeneous disorder, in which at least ۶۰۰ genes participate. The present study aimed to identify the effect of genetic counseling and consanguinity marriage in Iranian families with sporadic mental disability. Materials and Methods: In this retrospective cross-sectional study, we examined ۱۵۱ families with a sporadic mental disability referred for genetic consultation to the Welfare Center of Sari city, North of Iran. Results: About ۴۱.۰۵% (n=۶۲) of the cases were consanguinity marriage. In this study, other diseases were also observed with ID. The following four types of consultations were also reviewed, most of which were Diagnostic Counseling (DC) (۶۰%). According to the inheritance pattern analysis, the share of non-hereditary cases was higher compared to the share of hereditary and unknown cases. The results of the present study showed a significant difference between consanguinity marriages and potential genetic etiology ID (P=۰.۰۱۲). Besides, there was no significant difference between other groups. Conclusion: In this study, we highlighted the importance of genetic counseling and found that consanguinity marriage was a key factor in the development of the disease in our society. Therefore, given the high cost of genetic tests and socio-economic problems, it is wise to include genetic counseling to prevent many diseases such as mental disability before birth.

نویسندگان

Farzad Dastaviz

Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran.

Mohammad Bagher Hashemi- Soteh

Department of Clinical Biochemistry and Genetics, Molecular and Cell Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Peyman Aghabararian

Student Research Committee, Mazandaran University of Medical Sciences, Sari, Iran.

Saeed Zareei

Student Research Committee, Mazandaran University of Medical Sciences, Sari, Iran.

Saeed Dorgaleleh

Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran.

Moosa Rajabi Vandchali

Sari Genetic Counseling Center, Welfare Office, Mazandaran, Iran.

Mahsa Ghasempisheh

Sari Genetic Counseling Center, Welfare Office, Mazandaran, Iran.

Morteza Oladnabi

Gorgan Congenital Malformations Research Center, Golestan University of Medical Sciences, Gorgan, Iran AND Stem Cell Research Center, Golestan University of Medical Sciences, Gorgan, Iran AND Ischemic Disorders Research Center, Golestan University

Abouzar Bagheri

Department of Clinical Biochemistry and Genetics, Molecular and Cell Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.