International Journal of Molecular and Cellular Medicine (IJMCM)
Babol University of Medical Sciences
Mon, Jun 30, 2025
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Volume 5, Issue 1 (Int J Mol Cell Med 2016)
Int J Mol Cell Med 2016, 5(1): 57-64 |
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Sanyal D, Bhairi V, S Kadandale J. Practice of Consanguinity and Unusual Cases of Inherited Familial Chromosome Abnormalities: A Case Report. Int J Mol Cell Med 2016; 5 (1) :57-64
URL: http://ijmcmed.org/article-1-433-en.html
URL: http://ijmcmed.org/article-1-433-en.html
1- Lilac Insight Pvt Ltd, Ambience Court, 19th Floor, Unit 1901 & 1902, Sec-19 Vashi, Navi Mumbai 400705 Maharashtra, India. , jupiterdev@gmail.com
2- Lilac Insight Pvt Ltd, Ambience Court, 19th Floor, Unit 1901 & 1902, Sec-19 Vashi, Navi Mumbai 400705 Maharashtra, India.
3- Centre For Human Genetics, Biotech Park, Electronic City, Phase- I, Bangalore-560100, Karnataka, India.
2- Lilac Insight Pvt Ltd, Ambience Court, 19th Floor, Unit 1901 & 1902, Sec-19 Vashi, Navi Mumbai 400705 Maharashtra, India.
3- Centre For Human Genetics, Biotech Park, Electronic City, Phase- I, Bangalore-560100, Karnataka, India.
Abstract: (9275 Views)
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. In case 2, a couple was presented with 2nd degree consanguineous marriage and referred for 2 recurrent/ missed abortions. The amounts of shared genes are suggestive of more lethal genetic outcomes and inferred endogamy is a major driver to reproductive fiascoes, the ancestries of which are deeply tied at the meiotic level.
Type of Study: Case Report |
Subject:
Genetics & Disease
Received: 2015/12/18 | Accepted: 2016/02/3 | Published: 2016/03/7
Received: 2015/12/18 | Accepted: 2016/02/3 | Published: 2016/03/7
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