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Frequency and pattern of cytogenetic alterations in primary amenorrhea cases of Kashmir, North India
المؤلفون المشاركون
Pandith, Arshad A.
Dar, Fayaz A.
Zargar, Mahrukh H.
Malla, Tahir M.
المصدر
The Egyptian Journal of Medical Human Genetics
العدد
المجلد 17، العدد 1 (31 يناير/كانون الثاني 2016)، ص ص. 25-31، 7ص.
الناشر
الجمعية المصرية للأمراض الوراثية
تاريخ النشر
2016-01-31
دولة النشر
مصر
عدد الصفحات
7
التخصصات الرئيسية
الملخص EN
Background: Primary amenorrhea (PA) is proposed to have multiple etiological factors that include genetic factors, intrauterine malformations, endocrine dysfunction and environmental factors, as revealed by previous studies pertaining to amenorrhea.
However, among the various proposed etiologies, genetic factors appear to be highly associated with PA as approximately 40% of PA cases have been found to have genetic causes.
Aim of the study: The present study was proposed to establish the frequency and pattern of chromosomal abnormalities in PA cases of Kashmir.
Subjects and methods: A total of 108 females within the age group of 14–33 years and having a history of amenorrhea were included in the study.
Peripheral blood lymphocyte cultures were set for each subject according to standard protocol and chromosomal analysis was carried out on well spread metaphases by the help of Cytovision software Version 3.9.
Results: The results of the present study reveal that the incidence of chromosomal abnormalities in PA cases of this region is almost similar with those of many reports around the world.
However, we report two unique chromosomal alterations viz., 46,XX, dup2q(13) and 46,XX, t(2,5)(p11.2;q34) that have not been found elsewhere in the literature.
Conclusion: The results of the present study indicate that chromosomal analysis of females with PA, after the exclusion of non-genetic causes, should be essentially considered for the precise diagnosis and the development of more successful treatment.
The study being the first of its kind in this part of the world forms the basis for further studies of the PA cases of this region.
The precise molecular characterization of the unique breakpoint regions reported in our study can possibly help in the identification of new genes involved in primary amenorrhea.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Malla, Tahir M.& Dar, Fayaz A.& Pandith, Arshad A.& Zargar, Mahrukh H.. 2016. Frequency and pattern of cytogenetic alterations in primary amenorrhea cases of Kashmir, North India. The Egyptian Journal of Medical Human Genetics،Vol. 17, no. 1, pp.25-31.
https://search.emarefa.net/detail/BIM-655179
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Malla, Tahir M.…[et al.]. Frequency and pattern of cytogenetic alterations in primary amenorrhea cases of Kashmir, North India. The Egyptian Journal of Medical Human Genetics Vol. 17, no. 1 (Jan. 2016), pp.25-31.
https://search.emarefa.net/detail/BIM-655179
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Malla, Tahir M.& Dar, Fayaz A.& Pandith, Arshad A.& Zargar, Mahrukh H.. Frequency and pattern of cytogenetic alterations in primary amenorrhea cases of Kashmir, North India. The Egyptian Journal of Medical Human Genetics. 2016. Vol. 17, no. 1, pp.25-31.
https://search.emarefa.net/detail/BIM-655179
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references : p. 30-31
رقم السجل
BIM-655179
قاعدة معامل التأثير والاستشهادات المرجعية العربي "ارسيف Arcif"
أضخم قاعدة بيانات عربية للاستشهادات المرجعية للمجلات العلمية المحكمة الصادرة في العالم العربي
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