Preview

Medical Genetics

Advanced search

Analysis of pedigrees with a non-syndromic sensorineural hearing loss in assortative marriages

https://doi.org/10.25557/2073-7998.2018.05.47-50

Abstract

Nonsyndromic sensorineural hearing loss (NSHL) is a hereditary hearing impairment without other pathological symptoms (isolated), caused by damage to the sound-perceiving apparatus. NSHL is genetically heterogeneous, but on average, about 50% of cases of autosomal recessive NSHL is caused by mutations in the GJB2 gene. Marriages between hard-of-hearing people are a common occurrence in modern society, and the number of such marriages is increasing every year. At the same time, a growing interest in genetic testing was shown in couples consisting of assortative deaf marriages. On the example of two pedigrees, in which several assortative marriages were observed, the problems of medical genetic counseling of patients with hearing loss are analyzed taking into account the possibilities of confirmatory DNA diagnosis. The importance of molecular genetic examination for clarifying the form of the disease and determining the genetic risk for different types of marriages is demonstrated.

About the Authors

N. E. Petrina
Research Centre for Medical Genetics
Russian Federation


R. A. Zinchenko
Research Centre for Medical Genetics; Pirogov Russian National Research Medical University
Russian Federation


V. L. Izhevskaya
Research Centre for Medical Genetics
Russian Federation


A. V. Marakhonov
Research Centre for Medical Genetics; Moscow Institute of Physics and Technology (State University)
Russian Federation


E. A. Bliznetz
Research Centre for Medical Genetics
Russian Federation


N. A. Petrova
Research Centre for Medical Genetics
Russian Federation


T. A. Vasilyeva
Research Centre for Medical Genetics
Russian Federation


A. V. Polyakov
Research Centre for Medical Genetics
Russian Federation


E. K. Ginter
Research Centre for Medical Genetics
Russian Federation


References

1. Близнец Е.А., Галкина В.А., Матющенко Г.Н. и др. Изменения в гене коннексина 26 - GJB2 - при нарушениях слуха у российских пациентов: результаты многолетней молекулярной диагностики наследственной несиндромальной тугоухости. Генетика. 2012;48:110-121.

2. Morton C.C., Nance W.E. Newborn hearing screening - a silent revolution. N. Engl. J. Med. 2006;354(20):2151-2164. DOI 10.1056/ NEJMra050700

3. Petit, C., Levilliers, J. & Hardelin, J. Molecular genetics of hearing loss. Annu. Rev.Genet. 35, 589-646 (2001).

4. Kenneson, A., Van Naarden Braun, K. & Boyle, C. GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review. Genet. Med. 4, 258-274 (2002).

5. The Human Gene Mutation Database HGMD Professional 2017.3 http://www.hgmd.cf.ac.uk/ac/, дата последнего обращения 21.11.2017.

6. Посух О.Л., Бады-Хоо М.С., Зыцарь М.В. и др. Роль социально-демографической структуры сообществ глухих людей в распространенности наследуемых форм потери слуха. Вавиловский журнал генетики и селекции. 2016;20(1):7-15. DOI 10.18699/VJ16/098

7. Nance W.E., Kearsey M.J. Relevance of connexin deafness (DFNB1) to human evolution. Am. J. Hum. Genet. 2004;74(6):1081-1087. DOI 10.1086/420979

8. Middleton A, Hewison J, Mueller RF: Attitudes of deaf adults toward genetic testing for hereditary deafness. Am J Hum Genet 1998,63:1175-1180

9. Middleton A, Hewison J, Mueller R: Prenatal diagnosis for inherited deafness: what is the potential demand? J Genet Couns 2001, 10:121-131

10. Martinez A, Linden J, Schimmenti LA, et al. Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness. Genet Med 2003, 5:106-112

11. Tekin M., Xia X.J., Erdenetungalag R., et al. GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf // Ann. Hum. Genet. - 2010. - Vol. 74. - P. 155-164.

12. Teryutin F.M., Barashkov N.A., Kunel’skaya N.L., et al. The audiological analysis in the patients homozygous for the c.-23+1G>A mutation in the GJB2 gene presenting with the loss of hearing in Yakutiya. Vestn Otorinolaringol 2016;81(1):19-24.

13. Cryns K, Orzan E, Murgia A, et al. A genotype-phenotype correlation for GJB2 (connexin 26) deafness. J Med Genet. 2004 Mar; 41(3):147-54.

14. Rikkert L. Snoeckx, Patrick L., et al. GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study. Am. J. Hum. Genet. 2005;77:945-957.

15. Петрина Н.Е., Близнец Е.А., Зинченко Р.А., Макаов А.Х.-М., Петрова Н.В., Васильева Т.А., Чудакова Л.В., Петрин А.Н., Поляков А.В., Гинтер Е.К. Частота мутаций гена GJB2 у больных наследственной несиндромальной нейросенсорной тугоухостью в девяти популяциях Карачаево-Черкесской республики. Медицинская генетика. 2017;16(2):19-25.

16. Современное медико-генетическое консультирование / под ред. Е.К.Гинтера, С.И. Козловой. М.: Авторская Академия, 2016. 304с.


Review

For citations:


Petrina N.E., Zinchenko R.A., Izhevskaya V.L., Marakhonov A.V., Bliznetz E.A., Petrova N.A., Vasilyeva T.A., Polyakov A.V., Ginter E.K. Analysis of pedigrees with a non-syndromic sensorineural hearing loss in assortative marriages. Medical Genetics. 2018;17(5):47-50. (In Russ.) https://doi.org/10.25557/2073-7998.2018.05.47-50

Views: 685


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2073-7998 (Print)