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study of chromosomal abnormalities in couples with recurrent miscarriage in zahedan, iran
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نویسنده
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narooie-nejad mehrnaz ,nezam-abadi somayeh ,ranaei morad-ali ,bagherzade-yazdi mahdie ,mokhtari mojgan
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منبع
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gene cell tissue - 2017 - دوره : 4 - شماره : 2 - صفحه:1 -4
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چکیده
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Kground: recurrent miscarriage (rm) is defined as the presence of two or more spontaneous abortions. it has been estimated that 1% to 3% of couples experiencerm.furthermore,rmis considered as a multifactorial diseaseandgenetic disorders areoneof the suggested issues. in this study, 30 couples with rm were evaluated for their karyotypes, for the first time in sistan and baluchestan province. methods: in this study, 60 individuals (30 couples) with a history of recurrent miscarriage were recruited for cytogenetic evaluation through karyotyping of peripheral blood. all the participants in this study took part in immunologic, hematologic, and anatomic evaluations and no abnormality was found. results: among all male and female subjects of this study, only 2 females (6.7%) showed chromosomal aberration: mos45, x(3)/46xx(47) and 46, xx, and inv (8)(p12q21). both of these females had no children with a record of 3 miscarriages. these females and their partners had no history of miscarriage in their family. conclusions: the number of chromosomal abnormalities found in this study (6.7%) was less than other studies conducted in iran, including the city of mashad, yazd, tehran, and ahvaz. this might be because of the low number of participants taking part in this investigation. therefore, it is a necessity to perform furhter evaluations in this regard.
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کلیدواژه
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recurrent miscarriage ,chromosomal disorders ,karyotype
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آدرس
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zahedan university of medical sciences, genetic of non-communicable disease research center, genetics department, ایران, university of medical sciences, school of medicine, department of obstetrics and gynecology, ایران, zahedan university of medical sciences, aliasghar hospital, genetics laboratory, ایران, zahedan university of medical sciences, aliasghar hospital, genetics laboratory, ایران, university of medical sciences, school of medicine, department of obstetrics and gynecology, ایران
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پست الکترونیکی
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mmokhtari1345@hotmail.com
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Authors
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