Literature DB >> 24046181

Genetic screening services provided in Turkey.

Yurdagül Erdem1, Fulya Tekşen.   

Abstract

In Turkey, the rate of consanguineous marriage is quite high (22-24 %) and as a result, the incidence of autosomal recessive diseases and congenital anomalies is also very high and gives rise to a serious public health problem. In the last three decades, great effort has been made to avoid increases in the prevalence of these hereditary diseases. For this purpose, population-based premarital, prenatal, neonatal and adult genetic screening programs are performed in various centers such as Community Health Centers, Early Diagnosis of Cancer and Education Centers (KETEM), Prenatal and Neonatal Departments of Universities and State Hospitals and Thalessemia Screening Centers. Such centers are staffed by health professionals including physicians, family physicians, nurses, midwives, biologists and medical geneticists. Genetic counseling is also provided to patients attending these centers after screening tests are performed. Since there are no specialized training programs for genetic counselors, genetic counseling is generally provided by doctors or medical geneticists. The aim of this paper is to give an overview of the genetic screening services provided in Turkey, the prevalence of genetic diseases and the design of intensive educational programs for health professionals.

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Year:  2013        PMID: 24046181     DOI: 10.1007/s10897-013-9644-9

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  28 in total

1.  Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: roles of parental consanguinity and assortative mating.

Authors:  Mustafa Tekin; Türker Duman; Gönül Boğoçlu; Armağan Incesulu; Elif Comak; Inci Ilhan; Nejat Akar
Journal:  Hum Mutat       Date:  2003-05       Impact factor: 4.878

Review 2.  Application of medical genetics in Turkey.

Authors:  Ergül Tunçbilek; Meral Ozgüç
Journal:  Turk J Pediatr       Date:  2007 Oct-Dec       Impact factor: 0.552

3.  Alu insertion polymorphisms and an assessment of the genetic contribution of Central Asia to Anatolia with respect to the Balkans.

Authors:  Ceren Caner Berkman; Havva Dinc; Ceran Sekeryapan; Inci Togan
Journal:  Am J Phys Anthropol       Date:  2008-05       Impact factor: 2.868

4.  Prenatal diagnosis of sickle cell anemia and beta-thalassemia in southern Turkey.

Authors:  M Akif Cürük; Filiz Zeren; Ahmet Genç; Sezen Ozavci-Aygün; Yurdanur Kilinç; Kiymet Aksoy
Journal:  Hemoglobin       Date:  2008       Impact factor: 0.849

5.  What is the underlying cause of aneuploidy associated with increasing maternal age? Is it associated with elevated levels of gonadotropins?

Authors:  Polat Dursun; Murat Gultekin; Kunter Yuce; Ali Ayhan
Journal:  Med Hypotheses       Date:  2005-09-02       Impact factor: 1.538

6.  The moral implications of prenatal genetic testing.

Authors:  Peter Chipman
Journal:  Penn Bioeth J       Date:  2006

7.  Consanguineous marriage in Turkey and its impact on fertility and mortality.

Authors:  E Tunçbílek; I Koc
Journal:  Ann Hum Genet       Date:  1994-10       Impact factor: 1.670

8.  Breastfeeding and breast cancer risk by age 50 among women in Germany.

Authors:  J Chang-Claude; N Eby; M Kiechle; G Bastert; H Becher
Journal:  Cancer Causes Control       Date:  2000-09       Impact factor: 2.506

9.  Incidence of neural tube defects in Afyonkarahisar, Western Turkey.

Authors:  S T Onrat; H Seyman; M Konuk
Journal:  Genet Mol Res       Date:  2009-02-17

10.  Breast cancer in low- and middle-income countries: an emerging and challenging epidemic.

Authors:  Arafat Tfayli; Sally Temraz; Rachel Abou Mrad; Ali Shamseddine
Journal:  J Oncol       Date:  2010-12-15       Impact factor: 4.375

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  2 in total

1.  High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases.

Authors:  Semra Hiz Kurul; Yavuz Oktay; Ana Töpf; Nóra Zs Szabó; Serdal Güngör; Ahmet Yaramis; Ece Sonmezler; Leslie Matalonga; Uluc Yis; Katherine Schon; Ida Paramonov; İpek Polat Kalafatcilar; Fei Gao; Aliz Rieger; Nur Arslan; Elmasnur Yilmaz; Burcu Ekinci; Pinar Pulat Edem; Mahmut Aslan; Bilge Özgör; Angela Lochmüller; Ashwati Nair; Emily O'Heir; Alysia K Lovgren; Reza Maroofian; Henry Houlden; Kiran Polavarapu; Andreas Roos; Juliane S Müller; Denisa Hathazi; Patrick F Chinnery; Steven Laurie; Sergi Beltran; Hanns Lochmüller; Rita Horvath
Journal:  Brain       Date:  2022-05-24       Impact factor: 15.255

2.  Importance of multigene panel test in patients with consanguineous marriage and family history of breast cancer.

Authors:  Vahit Ozmen; Ahmet Okay Caglayan; Kanay Yararbas; Cetin Ordu; Fatma Aktepe; Tolga Ozmen; Ahmet Serkan Ilgun; Gursel Soybir; Gul Alco; Georgios N Tsaousis; Eirini Papadopoulou; Konstantinos Agiannitopoulos; Georgia Pepe; Stavroula Kampouri; George Nasioulas; Efe Sezgin; Atilla Soran
Journal:  Oncol Lett       Date:  2022-02-09       Impact factor: 2.967

  2 in total

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