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Naderi, Majid, Mirzaei, Ilia, Yaghoubi, Saeedeh, Azizi, Seyed Ghader. (1402). The Practicality of Family screening for Gaucher disease among first- and second-degree relatives: an effective diagnostic approach in high consanguinity. نشریه علمی دانشگاه سیستان و بلوچستان, (), -. doi: 10.22111/jep.2023.44665.1050
Majid Naderi; Ilia Mirzaei; Saeedeh Yaghoubi; Seyed Ghader Azizi. "The Practicality of Family screening for Gaucher disease among first- and second-degree relatives: an effective diagnostic approach in high consanguinity". نشریه علمی دانشگاه سیستان و بلوچستان, , , 1402, -. doi: 10.22111/jep.2023.44665.1050
Naderi, Majid, Mirzaei, Ilia, Yaghoubi, Saeedeh, Azizi, Seyed Ghader. (1402). 'The Practicality of Family screening for Gaucher disease among first- and second-degree relatives: an effective diagnostic approach in high consanguinity', نشریه علمی دانشگاه سیستان و بلوچستان, (), pp. -. doi: 10.22111/jep.2023.44665.1050
Naderi, Majid, Mirzaei, Ilia, Yaghoubi, Saeedeh, Azizi, Seyed Ghader. The Practicality of Family screening for Gaucher disease among first- and second-degree relatives: an effective diagnostic approach in high consanguinity. نشریه علمی دانشگاه سیستان و بلوچستان, 1402; (): -. doi: 10.22111/jep.2023.44665.1050

The Practicality of Family screening for Gaucher disease among first- and second-degree relatives: an effective diagnostic approach in high consanguinity

Journal of Epigenetics
مقالات آماده انتشار، پذیرفته شده، انتشار آنلاین از تاریخ 12 شهریور 1402
نوع مقاله: Original Article
شناسه دیجیتال (DOI): 10.22111/jep.2023.44665.1050
نویسندگان
Majid Naderi* 1؛ Ilia Mirzaei2؛ Saeedeh Yaghoubi3؛ Seyed Ghader Azizi4
1Genetics of Non-communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan Iran
2School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran. 3
3Department of Infectious Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
4Clinical Immunology Research Center, Zahedan University of Medical Sciences, Zahedan, Iran
چکیده
Gaucher Disease occurs more frequently in the offspring of familial marriages. With a wide variety of presentations, the long list of tests required to confirm GD in addition to those needed to rule out others puts a heavy financial burden on the patients, especially in regions where the majority live below the poverty line. Thus, in this study, we provide a familial screening method in patients whose relatives are confirmed GD cases, assuming that this approach might ease up the process.
In this study, 26 patients out of 217, whose family members were GD patients and had symptoms associated with GD were selected. Enzyme assay levels using Dried-Blood Samples from 3ml of samples were measured. Those with low levels of enzyme assay were further tested with GBA gene sequencing to confirm the diagnosis. The results of the sequencing revealed 5 carriers and 1 GD patient. Genetic counseling for GD on a personalized level is novel in the region, which all our patients received and responded positively to. In conclusion this process eases the diagnosis and reduces the overall burden of GD while keeping genetic counseling for the patients, which provides better care and opens up the possibilities of a registry system for GD patients and susceptible individuals in low-income countries.
کلیدواژه‌ها
Gaucher’s Disease؛ family screening؛ family history؛ cost-effectiveness؛ genetic counseling؛ genome sequencing
آمار
تعداد مشاهده مقاله: 20


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