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Literature DB >> 11765154

Clinical outcomes of consanguineous marriages in Turkey.

Abstract

Turkey has a high rate of consanguineous marriages. Different nationwide surveys indicate that today 20-25% of marriages are consanguineous, with the rate having increased over the last 15 years. The results of many studies show that the rate of consanguinity among parents of children with rare recessive diseases is quite above Turkey's average and that the high consanguinity rate is one of the underlying factors of high infant and child mortality and fertility in Turkey.

Entities: Disease Species

Mesh：

Year: 2001 PMID： 11765154

Source DB: PubMed Journal: Turk J Pediatr ISSN： 0041-4301 Impact factor: 0.552

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Cited

15 in total

1. Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib.

Authors: Serap Turan; Leyla Akin; Teoman Akcay; Erdal Adal; Sevil Sarikaya; Murat Bastepe; Harald Jüppner
Journal: Eur J Endocrinol Date: 2010-06-10 Impact factor: 6.664

2. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome.

Authors: Onur Cil; Nesrin Besbas; Ali Duzova; Rezan Topaloglu; Amira Peco-Antić; Emine Korkmaz; Fatih Ozaltin
Journal: Pediatr Nephrol Date: 2015-02-27 Impact factor: 3.714

3. Midwives' approach to genetic diseases and genetic counseling in Denizli, Turkey.

Authors: Ayşe Gaye Tomatir; Aysun Ozşahin; Hülya Cetin Sorkun; Huriye Demirhan; Beyza Akdağ
Journal: J Genet Couns Date: 2006-06 Impact factor: 2.537

4. Further defining the clinical and molecular spectrum of acromesomelic dysplasia type maroteaux: a Turkish tertiary center experience.

Authors: Pelin Ozlem Simsek-Kiper; Gizem Urel-Demir; Ekim Z Taskiran; Umut Ece Arslan; Banu Nur; Ercan Mihci; Mithat Haliloglu; Yasemin Alanay; Gulen Eda Utine; Koray Boduroglu
Journal: J Hum Genet Date: 2020-12-07 Impact factor: 3.172

Review 5. Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings.

Authors: C Geoffrey Woods; Jacquelyn Bond; Wolfgang Enard
Journal: Am J Hum Genet Date: 2005-03-31 Impact factor: 11.025

Review 6. The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.

Authors: Ayşegül Ozantürk; Jan D Marshall; Gayle B Collin; Selma Düzenli; Robert P Marshall; Şükrü Candan; Tülay Tos; İhsan Esen; Mustafa Taşkesen; Atilla Çayır; Şükrü Öztürk; İhsan Üstün; Esra Ataman; Emin Karaca; Taha Reşid Özdemir; İlknur Erol; Fehime Kara Eroğlu; Deniz Torun; Erhan Parıltay; Elif Yılmaz-Güleç; Ender Karaca; M Emre Atabek; Nursel Elçioğlu; İlhan Satman; Claes Möller; Jean Muller; Jürgen K Naggert; Rıza Köksal Özgül
Journal: J Hum Genet Date: 2014-10-09 Impact factor: 3.172

Clinical outcomes of consanguineous marriages in Turkey.

1. Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib.

2. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome.

3. Midwives' approach to genetic diseases and genetic counseling in Denizli, Turkey.

4. Further defining the clinical and molecular spectrum of acromesomelic dysplasia type maroteaux: a Turkish tertiary center experience.

Review 5. Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings.

Review 6. The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.

7. Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families.

8. Haematological findings in children with inborn errors of metabolism.

9. Familial mediterranean Fever: a retrospective clinical and molecular study in the East of anatolia region of Turkey.

10. Does maternal knowledge impact blood phenylalanine concentration in Turkish children with phenylketonuria?