Literature DB >> 21221751

Reasons for adult referrals for genetic counseling at a genetics center in Izmir, Turkey: analysis of 8965 cases over an eleven-year period.

Ozgur Cogulu1, Ferda Ozkinay, Haluk Akin, Huseyin Onay, Emin Karaca, Asude Alpman Durmaz, Burak Durmaz, Ayca Aykut, Erhan Pariltay, Ozgur Kirbiyik, Cumhur Gunduz, Cihangir Ozkinay.   

Abstract

A limited numbers of published studies evaluate the referral reasons for genetic counseling services in the literature. These studies are focused on prenatal genetic counseling services, in particular, prenatal diagnosis. In order to provide the most effective and helpful genetic counseling services, genetics professionals need adequate knowledge about the profile of individuals referred for these services. In addition, physicians need increased awareness of the nature of genetic issues in order to make appropriate referrals. This study was intended to provide a descriptive analysis of the referral reasons of patients that received genetic counseling at a genetics center in Izmir, Turkey during an 11-year period. A total of 8965 records generated between 1998 and 2008 from one genetic center (which consists of The Department of Medical Genetics and Division of Pediatric Genetics) were evaluated retrospectively. Of these, 6,258 involved referrals for prenatal reasons, and 2,707 involved referrals for postnatal reasons. Both prenatal and postnatal records were further classified into more specific categories of referral reasons. The most common reason for genetic counseling among the prenatal patients was advanced maternal age (42.0%), followed by high risk results on prenatal biochemical screening tests such as second trimester double test [(serum concentration of alphafetoprotein (AFP), beta-human chorionic gonadotropin (beta-HCG)], triple test (serum concentration of AFP, beta-HCG, oestriol) and integrated test (26.5%). The most common indications for postnatal patients were recurrent miscarriages (28.2%) and infertility (19.7%). A significant increase in number of specific categories of referrals for genetic counseling was observed for the last 3 years after the establishment of the Medical Genetics Department. These data provide useful information about the frequency of referrals to the genetics department, and the feasibility of genetic services. Organization of genetic services and systematic procedures for genetic counseling and genetic testing may improve the public's awareness of genetics and ensure a high standard of patient care.

Entities:  

Mesh:

Year:  2011        PMID: 21221751     DOI: 10.1007/s10897-010-9342-9

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


  18 in total

Review 1.  Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE).

Authors:  Lihadh Al-Gazali; Bassam R Ali
Journal:  Hum Mutat       Date:  2010-05       Impact factor: 4.878

2.  The role of genetic counseling on decisions of pregnant women aged 35 years or over regarding amniocentesis in Turkey.

Authors:  Hatice Ilgin-Ruhi; Nüket Yürür-Kutlay; Ajlan Tükün; Işik Bökesoy
Journal:  Eur J Med Genet       Date:  2005-02-01       Impact factor: 2.708

3.  A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.

Authors:  Robert Resta; Barbara Bowles Biesecker; Robin L Bennett; Sandra Blum; Susan Estabrooks Hahn; Michelle N Strecker; Janet L Williams
Journal:  J Genet Couns       Date:  2006-04       Impact factor: 2.537

Review 4.  Guidelines for molecular karyotyping in constitutional genetic diagnosis.

Authors:  Joris Robert Vermeesch; Heike Fiegler; Nicole de Leeuw; Karoly Szuhai; Jacqueline Schoumans; Roberto Ciccone; Frank Speleman; Anita Rauch; Jill Clayton-Smith; Conny Van Ravenswaaij; Damien Sanlaville; Philippos C Patsalis; Helen Firth; Koen Devriendt; Orsetta Zuffardi
Journal:  Eur J Hum Genet       Date:  2007-07-18       Impact factor: 4.246

5.  The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.

Authors:  A Nazi Basak
Journal:  Hemoglobin       Date:  2007       Impact factor: 0.849

6.  Analysis of clinical features predicting etiologic yield in the assessment of global developmental delay.

Authors:  Myriam Srour; Barbara Mazer; Michael I Shevell
Journal:  Pediatrics       Date:  2006-07       Impact factor: 7.124

7.  Genetic testing: a physician's perspective.

Authors:  J D Menasha; C Schechter; J Willner
Journal:  Mt Sinai J Med       Date:  2000-03

8.  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

Review 9.  Genetic risk assessment, counseling and testing.

Authors:  Thereasa A Rich; Mary Salazar
Journal:  Surg Oncol Clin N Am       Date:  2009-01       Impact factor: 3.495

10.  Patient follow-up is a major problem at genetics clinics.

Authors:  Carmen Esmer; Nora Urraca; Alessandra Carnevale; Victoria Del Castillo
Journal:  Am J Med Genet A       Date:  2004-03-01       Impact factor: 2.802

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.