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JCR 2016
جستجوی مقالات
شنبه 22 آذر 1404
Iranian Journal of Medical Sciences
، جلد ۴۴، شماره ۳، صفحات ۲۶۲-۰
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Hereditary Ataxia with a Novel Mutation in the Senataxin Gene: A Case Report
چکیده انگلیسی مقاله
Hereditary ataxias (HA) are a group of inherited neurological disorders caused by changes in genes. At least 115 different mutations in the senataxin (SETX) gene causing ataxia have been identified. There are no reports of any SETX gene mutation among the Iranian population. Here we report on two cases with homozygous and heterozygous mutations in which one patient was affected by HA with oculomotor apraxia type 2, and the other was a carrier of the disorder. In 2016, the affected patient was referred to the Biogene Medical and Genetic Laboratory (Tehran, Iran) suffering from imbalance and tremor of both head and body. The coding regions of 18 genes, including the SETX gene, were screened. The target regions were captured using the NimbleGen chip followed by next-generation sequencing (NGS) technology on the Illumina Hiseq2500 platform. NGS, a DNA sequencing technology, has greatly increased the ability to identify new causes of ataxia; a useful tool for the prevention of primary manifestations and treatment of affected patients. In the present study, a novel mutation in the SETX gene has been identified
کلیدواژههای انگلیسی مقاله
نویسندگان مقاله
| Ehsan Moghanloo
Biogene Medical and Genetic Laboratory, Tehran, Iran
| Ziba Morovvati
Department of Biotechnology, Bu-Ali sina University, Hamedan, Iran
| Maghsoud Seifi
Human Genetics Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
| Fatemeh Minoochehr
Human Genetics Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
| Saeid Morovvati
Department of Medical Genetics, Iran University of Medical Sciences, Tehran, Iran
| Shahram Teimourian
نشانی اینترنتی
http://ijms.sums.ac.ir/index.php/IJMS/article/view/5165
فایل مقاله
اشکال در دسترسی به فایل - ./files/site1/rds_journals/147/article-147-1464472.pdf
کد مقاله (doi)
زبان مقاله منتشر شده
en
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نوع مقاله منتشر شده
Case Report(s)
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