دورية أكاديمية
أعرض في EDS

A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia.

التفاصيل البيبلوغرافية
العنوان: A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia.
المؤلفون: Romanov GP; Laboratory of Molecular Biology, MK Ammosov North-Eastern Federal University, Yakutsk, Russia.; Laboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russia., Pshennikova VG; Laboratory of Molecular Biology, MK Ammosov North-Eastern Federal University, Yakutsk, Russia.; Laboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russia., Lashin SA; Federal Research Center Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.; Novosibirsk State University, Novosibirsk, Russia., Solovyev AV; Laboratory of Molecular Biology, MK Ammosov North-Eastern Federal University, Yakutsk, Russia.; Laboratory of the Human in the Arctic, Institute for Humanitarian Research and North Indigenous Peoples Problems, Federal Research Centre 'The Yakut Scientific Centre of the Siberian Branch of the Russian Academy of Sciences', Yakutsk, Russia., Teryutin FM; Laboratory of Molecular Biology, MK Ammosov North-Eastern Federal University, Yakutsk, Russia.; Laboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russia., Cherdonova AM; Laboratory of Molecular Biology, MK Ammosov North-Eastern Federal University, Yakutsk, Russia., Borisova TV; Laboratory of Molecular Biology, MK Ammosov North-Eastern Federal University, Yakutsk, Russia., Sazonov NN; Laboratory of Molecular Biology, MK Ammosov North-Eastern Federal University, Yakutsk, Russia., Khusnutdinova EK; Laboratory of Human Molecular Genetics, Institute of Biochemistry and Genetics, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russia.; Department of Genetics and Fundamental Medicine, Bashkir State University, Ufa, Russia., Posukh OL; Federal Research Center Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.; Novosibirsk State University, Novosibirsk, Russia., Fedorova SA; Laboratory of Molecular Biology, MK Ammosov North-Eastern Federal University, Yakutsk, Russia.; Laboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russia., Barashkov NA; Laboratory of Molecular Biology, MK Ammosov North-Eastern Federal University, Yakutsk, Russia.; Laboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russia.
المصدر: PloS one [PLoS One] 2020 Nov 30; Vol. 15 (11), pp. e0242219. Date of Electronic Publication: 2020 Nov 30 (Print Publication: 2020).
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
أسماء مطبوعة: Original Publication: San Francisco, CA : Public Library of Science
مواضيع طبية MeSH: Sign Language*, Deafness/*epidemiology, Censuses ; Deafness/congenital ; Humans ; Prevalence ; Russia/epidemiology
مستخلص: The absence of comparable epidemiological data challenges the correct estimation of the prevalence of congenital hearing loss (HL) around the world. Sign language (SL) is known as the main type of communication of deaf people. We suggest that the distribution of SL can be interpreted as an indirect indicator of the prevalence of congenital HL. Since a significant part of congenital HL is due to genetic causes, an assessment of the distribution of SL users can reveal regions with an extensive accumulation of hereditary HL. For the first time, we analyzed the data on the distribution of SL users that became available for the total population of Russia by the 2010 census. Seventy-three out of 85 federal regions of Russia were ranked into three groups by the 25th and 75th percentiles of the proportion of SL users: 14 regions-"low proportion"; 48 regions-"average proportion"; and 11 regions-"high proportion". We consider that the observed uneven prevalence of SL users can reflect underlying hereditary forms of congenital HL accumulated in certain populations by specific genetic background and population structure. At least, the data from this study indicate that the highest proportions of SL users detected in some Siberian regions are consistent with the reported accumulation of specific hereditary HL forms in indigenous Yakut, Tuvinian and Altaian populations.
Competing Interests: The authors have declared that no competing interests exist.
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تواريخ الأحداث: Date Created: 20201130 Date Completed: 20201231 Latest Revision: 20240330
رمز التحديث: 20240330
مُعرف محوري في PubMed: PMC7703874
DOI: 10.1371/journal.pone.0242219
PMID: 33253245
قاعدة البيانات: MEDLINE
الوصف
تدمد:1932-6203
DOI:10.1371/journal.pone.0242219