|
Frenny J Sheth describes for SIIC the most significant aspects of his article describe para SIIC los aspectos relevantes de su artículo Genetic alterations as a cause for recurrent miscarriages CHROMOSOMAL REARRANGEMENTS AND COUNSELING IN CASES WITH REPEATED FETAL WASTAGE Chromosomal anomalies are one of the underlying bases of reproductive failure. Comprehensive characterization and association analysis of gross anomalies, variants and marker chromosomes could aid in recurrence risk calculation for subsequent pregnancy. Cytogenetic analysis of couples with reduced reproductive fitness and recurrent abortions would facilitate counseling and patient management. The article was published by El artículo fue publicado por
Principal institution where the research took place Institución principal de la investigación FRIGE's Institute of Human Genetics, Ahmedabad, Gujarat, India  Authors' Report Crónica del Autor Bibliographic references Referencias bibliográficas Al Hussain M, Al-Nuaim L, Talib ZA, Zaki OK. Cytogenetic study in cases with recurrent abortion in Saudi Arabia. Ann Saudi Med 20:233-236, 2000. An International System for Human CytogeneticNomenclature. In: Karger S, Basel JC, editors. Shaffer LG, McGowan-Jordan J, Schmid M; 2013. Dubey S, Chowdary MR, Prahlad B, Kumar V, Mathur R, Hamilton S, et al. Cytogenetic causes for recurrent spontaneous abortion-An experience of 742 couples (1 484 cases). Indian J Hum Genet 11:94-98, 2005. Dutta UR, Rajitha P, Pidugu VK, Dalal AB. Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in southern region of India: Report and review. J Assist Reprod Genet 28:145-149, 2011. Fryns JP, Van Buggenhout G. Structural chromosome rearrangements in couples with recurrent fetal wastage. Eur J Obstet Gynecol Reprod Biol 81:171-176, 1998. Jauniaux E, Farquharson RG, Christiansen OB, Exalto N. Evidence-based guidelines for the investigation and medical treatment of recurrent miscarriage. Hum Reprod 21:2216-2222, 2006. Krishna DS, AL-Awadi SA, Farag TI: Pericentric inversion and recombinant aneusomy and other associated chromosomal aberrations: random or non-random. Am J Hum Genet 51:A291(1146), 1992. Kumar M, Thatai A, Chapadgaonkar SS: Homozygosity and Heterozygosity of the Pericentric Inversion of Chromosome 9 and Its Clinical Impact. J Clin Diagn Res 6:816-820, 2012. Madon PF, Athalye AS, Parikh FR: Polymorphic variants on chromosomes probably play a significant role in infertility. Reprod Biomed Online 11:726-732, 2005. Manvelyan M, Schreyer I, Höls-Herpertz I, Köhler S, Niemann R, Hehr U, et al. Forty-eight new cases with infertility due to balanced chromosomal rearrangements: detailed molecular cytogenetic analysis of the 90 involved breakpoints. Int J Mol Med 19:855-864, 2007. Meza-Espinoza JP, Anguiano LO, Rivera H. Chromosomal abnormalities in couples with reproductive disorders. Gynecol Obstet Invest 66:237-240, 2008. Motos Guirao MA. Pericentric inversion of the human Y chromosome. An Esp Pediatr 31:583-587, 1989. Practice Committee of the American Society for Reproductive Medicine. Evaluation and treatment of recurrent pregnancy loss: A committee opinion. Fertil Steril 98:1103-1111, 2012. Rajangam S, Tilak P, Aruna N, Devi R. Karyotyping and counseling in bad obstetric history and infertility. Iran J Reprod Med 5:7-12, 2007. Rybouchkin A, Benijts J, DeSutter P, Dhond M. Disintegration of chromosomes in dead sperm cells as revealed by injection into mouse oocytes. Hum Reprod 12:1693-1698, 1997. Shafeghati Y, Karimi Nejad M, Zangeneh M, Karimi Nejad R, Baba Mohammadi Q, Almadani N, et al. Results of chromosome studies in 664 Iranian couples with the history of recurrent early pregnancy loss. Abstract in European Human Genetics Conference. European Society of Human Genetics: Strasbourg, France. P. 5; 2002. Sheth FJ, Shah UJ, Desai M, Sheth JJ. Clinical profile of inversion Y in people of Gujarat, West India. Int J Hum Genet 11:245-248, 2011. Zhou B, Tang YP, Liu YZ. Mechanism of the formation of a special inv(Y): a case study. Yi Chuan 28:148-152, 2006. Other articles written by the author Frenny J Sheth Otros artículos de Frenny J Sheth • R Asadollahi, B Oneda, F Sheth, S Azzarello-Burri, R Baldinger, P Joset, B Latal, W Knirsch, S Desai, A Baumer, G Houge, J Andrieux, A Rauch (2013). Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability. EJHG 21(10):1100-1104. • F Sheth, O Akinde, C Datar , O Adeteye, J Sheth (2012).Genotype-phenotype characterization of wolf-Hirschhorn syndrome confirmed by FISH - case reports. Case Rep Genet.:878796. doi: 10.1155/2012/878796 • F Sheth, N Gohel, T Liehr, O Akinde, M Desai, O Adeteye, J Sheth (2012). Gain of chromosome 4qter and loss of 5pter – an unusual case with features of Cri du chat syndrome (CdCS). Case Reports in Genetics. vol. 2012, Article ID 153405, 4 pages, doi:10.1155/2012/153405 • F Sheth, J Andrieux, E Ewers, N Kosyakova, A Weise, H Sheth, S Romana, M Lorch, B Deloben, O Theisen, T Liehr, S Numpoothiri, J Sheth (2011). Characterization of sSMC by FISH and molecular techniques. Euro J Med Genet. 54:247-255. • F Sheth, J Andrieux, J Sheth (2010). Marker chromosome in a child with microcephaly and mental retardation. Ind Pediatr. 47:277-279. • J Andrieux, F Sheth (2009). CGH-Array study and its utility in children for detection of Constitutional and Acquired anomalies. Ind J Exp Biol. 47:779-791. • F Sheth, E Ewers, N Kosyakova, A Weise, J Sheth, S Patil, M Ziegler, T Liehr (2009). A neocentric isochromosome Yp present as additional small supernumerary marker chromosome – evidence against U-type exchange mechanism? Cytogenetic Genome Research 125(2):115-116. • F Sheth, E Ewers, N Kosyakova, A Weise, J Sheth, M Desai, J Andrieux, J Vermeesch, M Ziegler, T Liehr (2009). Small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome – a case report. Molecular Cytogenet 2: 22. SIIC System of Assisted Editing (SSEA) / Sistema SIIC de Edición Asistida (SSEA)
The article is strictly related to the following sections of siicsalud El artículo se relaciona estrictamente con las siguientes secciones de siicsalud
Information about the full text Acerca del trabajo completo Chromosomal Abnormalities in Couples With Repeated Fetal Loss: An Indian Retrospective Study Author / Autor Frenny Sheth1, Frenny J Sheth2, Thomas Leihr3, Pritti Kumari4, Harsh Sheth5, Jayesh Sheth6, Thomas Leihr7, Pritti Kumari8, Harsh Sheth9, Jayesh Sheth10, Thomas Leihr11, Pritti Kumari12, Harsh Sheth13, Jayesh Sheth14, Thomas Leihr15, Pritti Kumari16, Harsh Sheth17, Jayesh Sheth18, Thomas Leihr19, Pritti Kumari20, Harsh Sheth21, Jayesh Sheth22 22 Dr., Frige’s Institute Of Human Genetics, Frige House, Satellite, Ahmedabad-380015. Gujarat.india., Chairman Access to the original source Indian Journal of Human Genetics Article URL: / URL del artículo: http://www.bioline.org.br/hg URL of Abstract page in Medline: / URL del abstract en Medline: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897136/?report=reader siic DB: / siic DB: http://www.siicsalud.com/main/distriprinrel.php |
||||||||||||||||||||||||||
Copyright siicsalud © 1997-2024 ISSN siicsalud: 1667-9008
