نتایج جستجو برای: consanguineous marriage

تعداد نتایج: 21283  

Journal: :Journal of biosocial science 2016
Bashir Ahmad Atta Ur Rehman Sajid Malik

The north-western populations of Pakistan in the Federally Administered Tribal Areas (FATA) adjoining the Pakistan-Afghanistan border are an amalgamation of native and migrated Pashtun tribes. These tribal populations are in transition due to war conditions and geo-political turmoil on both sides of the border since the Soviet invasion in 1979. Bio-demographic and epidemiological data for these...

لطفی, یونس, جعفری, زهرا , مهرکیان, سعیده ,

    Background & Aim: Consanguineous marriage is strongly favored in many large human populations. In most parts of South Asia, consanguineous marriage accounts for 20-50% of the total present generation. The effect of consanguinity on hereditary deafness has been well studied and documented. Many authors have suggested that approximately one half of sensory neural hearing loss in children can ...

Journal: :international journal of molecular and cellular medicine 0
debarshi sanyal lilac insight pvt ltd, ambience court, 19th floor, unit 1901 & 1902, sec-19 vashi, navi mumbai 400705 maharashtra, india. vidya bhairi lilac insight pvt ltd, ambience court, 19th floor, unit 1901 & 1902, sec-19 vashi, navi mumbai 400705 maharashtra, india. jayarama s kadandale centre for human genetics, biotech park, electronic city, phase- i, bangalore-560100, karnataka, india.

we present 2 cases of likely rare event. in case 1, 3rd degree consanguineous marriage revealed inv(6) with same break points in parents who were found to be phenotypically normal. the same inv(6) being inherited in progeny but presented with low amh (anti mullerian hormone) and high level of fsh (follicular stimulating hormone) leading to polycystic ovarian syndrome/premature ovarian failure. ...

Journal: :Japanese Journal of Health and Human Ecology 1950

We present 2 cases of likely rare event. In case 1, 3rd degree consanguineous marriage revealed inv(6) with same break points in parents who were found to be phenotypically normal. The same inv(6) being inherited in progeny but presented with low AMH (anti Mullerian hormone) and high level of FSH (follicular stimulating hormone) leading to polycystic ovarian syndrome/premature ovarian failure. ...

2015

Consanguineous couples are at increased risk of having a child with a hereditary/congenital disorder. This extra risk is caused by the fact that the child can inherit the same mutated allele from both parents that originates from a common ancestor. First cousin couples are said to have 1.7-2.8% extra risk on top of the background risk that every couple has of having a child with a congenital/he...

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