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The association between consanguineous marriage and offspring with congenital hearing loss
Consanguinity is a commonly recognized practice among marriages in the Middle East and may lead to an increase in the prevalence of inherited disorders. Autosomal recessive deafness is the most common form of inherited congenital hearing loss (CHL). Determine the association of consanguineous marria...
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Published in: | Annals of Saudi medicine 2020-11, Vol.40 (6), p.456-461 |
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creator | Almazroua, Aljohara M Alsughayer, Luluh Ababtain, Rayanh Al-Shawi, Yazeed Hagr, Abdulrahman A |
description | Consanguinity is a commonly recognized practice among marriages in the Middle East and may lead to an increase in the prevalence of inherited disorders. Autosomal recessive deafness is the most common form of inherited congenital hearing loss (CHL).
Determine the association of consanguineous marriages with congenital sensorineural hearing loss (SNHL) and auditory neuropathy.
Descriptive and analytical cross-sectional study.
Ear specialist hospital.
Children with severe-to-profound congenital SNHL, who had been referred to the specialist hospital for cochlear implant were analyzed. Patients were divided into subgroups based on degree of consanguinity.
The relative risk of having more than one child with SNHL in offspring of a consanguineous marriage.
189 parents and children with CHL.
The parents of 157 children (83.1%) were blood-related. Of those, 48 had more than one child with CHL (31.4%), while only two parents who were not blood-related had more than one child with CHL (6.25%;
=.005). Among the 189 children, 131 (69.3%) parents were direct cousins. Only 39 (20.6%) and 43 (22.8%) children had family histories of CHL on the paternal and maternal sides, respectively. There was no statistically significant difference in the prevalence of auditory neuropathy between the offspring of consanguineous and non-consanguineous marriages (
=.648).
The risk of having more than one child with SNHL in the offspring from a consanguineous marriage is 3.5 times higher than that of a non-consanguineous mating.
The association of hearing loss degree with consanguinity was not studied.
None. |
doi_str_mv | 10.5144/0256-4947.2020.456 |
format | article |
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Determine the association of consanguineous marriages with congenital sensorineural hearing loss (SNHL) and auditory neuropathy.
Descriptive and analytical cross-sectional study.
Ear specialist hospital.
Children with severe-to-profound congenital SNHL, who had been referred to the specialist hospital for cochlear implant were analyzed. Patients were divided into subgroups based on degree of consanguinity.
The relative risk of having more than one child with SNHL in offspring of a consanguineous marriage.
189 parents and children with CHL.
The parents of 157 children (83.1%) were blood-related. Of those, 48 had more than one child with CHL (31.4%), while only two parents who were not blood-related had more than one child with CHL (6.25%;
=.005). Among the 189 children, 131 (69.3%) parents were direct cousins. Only 39 (20.6%) and 43 (22.8%) children had family histories of CHL on the paternal and maternal sides, respectively. There was no statistically significant difference in the prevalence of auditory neuropathy between the offspring of consanguineous and non-consanguineous marriages (
=.648).
The risk of having more than one child with SNHL in the offspring from a consanguineous marriage is 3.5 times higher than that of a non-consanguineous mating.
The association of hearing loss degree with consanguinity was not studied.
None.</description><identifier>ISSN: 0256-4947</identifier><identifier>EISSN: 0975-4466</identifier><identifier>DOI: 10.5144/0256-4947.2020.456</identifier><identifier>PMID: 33307738</identifier><language>eng</language><publisher>Saudi Arabia: King Faisal Specialist Hospital and Research Centre</publisher><subject>Adult ; Child ; Child, Preschool ; Consanguinity ; Cross-Sectional Studies ; Deafness - epidemiology ; Deafness - genetics ; Female ; Hearing Loss, Sensorineural - congenital ; Humans ; Male ; Marriage - ethnology ; Middle East - epidemiology ; Original ; Pedigree ; Risk Factors</subject><ispartof>Annals of Saudi medicine, 2020-11, Vol.40 (6), p.456-461</ispartof><rights>Copyright © 2020, Annals of Saudi Medicine, Saudi Arabia 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-2995a0a112558ed9551a7fbba6eb5fc2d6b33f7a0a1e0b9063fc1c27201d9043</citedby><cites>FETCH-LOGICAL-c468t-2995a0a112558ed9551a7fbba6eb5fc2d6b33f7a0a1e0b9063fc1c27201d9043</cites><orcidid>0000-0002-8497-8326</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733643/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733643/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33307738$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Almazroua, Aljohara M</creatorcontrib><creatorcontrib>Alsughayer, Luluh</creatorcontrib><creatorcontrib>Ababtain, Rayanh</creatorcontrib><creatorcontrib>Al-Shawi, Yazeed</creatorcontrib><creatorcontrib>Hagr, Abdulrahman A</creatorcontrib><title>The association between consanguineous marriage and offspring with congenital hearing loss</title><title>Annals of Saudi medicine</title><addtitle>Ann Saudi Med</addtitle><description>Consanguinity is a commonly recognized practice among marriages in the Middle East and may lead to an increase in the prevalence of inherited disorders. Autosomal recessive deafness is the most common form of inherited congenital hearing loss (CHL).
Determine the association of consanguineous marriages with congenital sensorineural hearing loss (SNHL) and auditory neuropathy.
Descriptive and analytical cross-sectional study.
Ear specialist hospital.
Children with severe-to-profound congenital SNHL, who had been referred to the specialist hospital for cochlear implant were analyzed. Patients were divided into subgroups based on degree of consanguinity.
The relative risk of having more than one child with SNHL in offspring of a consanguineous marriage.
189 parents and children with CHL.
The parents of 157 children (83.1%) were blood-related. Of those, 48 had more than one child with CHL (31.4%), while only two parents who were not blood-related had more than one child with CHL (6.25%;
=.005). Among the 189 children, 131 (69.3%) parents were direct cousins. Only 39 (20.6%) and 43 (22.8%) children had family histories of CHL on the paternal and maternal sides, respectively. There was no statistically significant difference in the prevalence of auditory neuropathy between the offspring of consanguineous and non-consanguineous marriages (
=.648).
The risk of having more than one child with SNHL in the offspring from a consanguineous marriage is 3.5 times higher than that of a non-consanguineous mating.
The association of hearing loss degree with consanguinity was not studied.
None.</description><subject>Adult</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Consanguinity</subject><subject>Cross-Sectional Studies</subject><subject>Deafness - epidemiology</subject><subject>Deafness - genetics</subject><subject>Female</subject><subject>Hearing Loss, Sensorineural - congenital</subject><subject>Humans</subject><subject>Male</subject><subject>Marriage - ethnology</subject><subject>Middle East - epidemiology</subject><subject>Original</subject><subject>Pedigree</subject><subject>Risk Factors</subject><issn>0256-4947</issn><issn>0975-4466</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkc1u1DAUhS1ERcvAC7BAWbLJ4H-PN0ioaqFSJTaz6sa6ca4zrjJ2iTNUvD3OTFvRlS37u8fH5xDyidG1YlJ-pVzpVlpp1pxyupZKvyEX1BrVSqn127p_Bs7J-1LuaaWkEO_IuRCCGiM2F-Ruu8MGSsk-whxzajqcHxFT43MqkIZDTJgPpdnDNEUYKpv6JodQHqaYhuYxzrsFHTDFGcZmh3A8H3MpH8hZgLHgx6d1RbbXV9vLn-3trx83l99vWy_1Zm65tQooMMaV2mBvlWJgQteBxk4Fz3vdCRHMgiDtLNUieOa54ZT1tv5nRW5Osn2Ge1dtVat_XYbojgd5GhxMc_QjOssMWg1KsH4jg0JrefBG0uqjN9TaqvXtpPVw6PbYe0zzBOMr0dc3Ke7ckP-4GqbQNdsV-fIkMOXfByyz28ficRzhGKPj0lAqpGULyk-on2pYE4aXZxh1S79uqc8t9bmlX1f7rUOf_zf4MvJcqPgHEReiDA</recordid><startdate>20201101</startdate><enddate>20201101</enddate><creator>Almazroua, Aljohara M</creator><creator>Alsughayer, Luluh</creator><creator>Ababtain, Rayanh</creator><creator>Al-Shawi, Yazeed</creator><creator>Hagr, Abdulrahman A</creator><general>King Faisal Specialist Hospital and Research Centre</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-8497-8326</orcidid></search><sort><creationdate>20201101</creationdate><title>The association between consanguineous marriage and offspring with congenital hearing loss</title><author>Almazroua, Aljohara M ; Alsughayer, Luluh ; Ababtain, Rayanh ; Al-Shawi, Yazeed ; Hagr, Abdulrahman A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-2995a0a112558ed9551a7fbba6eb5fc2d6b33f7a0a1e0b9063fc1c27201d9043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Consanguinity</topic><topic>Cross-Sectional Studies</topic><topic>Deafness - epidemiology</topic><topic>Deafness - genetics</topic><topic>Female</topic><topic>Hearing Loss, Sensorineural - congenital</topic><topic>Humans</topic><topic>Male</topic><topic>Marriage - ethnology</topic><topic>Middle East - epidemiology</topic><topic>Original</topic><topic>Pedigree</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Almazroua, Aljohara M</creatorcontrib><creatorcontrib>Alsughayer, Luluh</creatorcontrib><creatorcontrib>Ababtain, Rayanh</creatorcontrib><creatorcontrib>Al-Shawi, Yazeed</creatorcontrib><creatorcontrib>Hagr, Abdulrahman A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Annals of Saudi medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Almazroua, Aljohara M</au><au>Alsughayer, Luluh</au><au>Ababtain, Rayanh</au><au>Al-Shawi, Yazeed</au><au>Hagr, Abdulrahman A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The association between consanguineous marriage and offspring with congenital hearing loss</atitle><jtitle>Annals of Saudi medicine</jtitle><addtitle>Ann Saudi Med</addtitle><date>2020-11-01</date><risdate>2020</risdate><volume>40</volume><issue>6</issue><spage>456</spage><epage>461</epage><pages>456-461</pages><issn>0256-4947</issn><eissn>0975-4466</eissn><abstract>Consanguinity is a commonly recognized practice among marriages in the Middle East and may lead to an increase in the prevalence of inherited disorders. Autosomal recessive deafness is the most common form of inherited congenital hearing loss (CHL).
Determine the association of consanguineous marriages with congenital sensorineural hearing loss (SNHL) and auditory neuropathy.
Descriptive and analytical cross-sectional study.
Ear specialist hospital.
Children with severe-to-profound congenital SNHL, who had been referred to the specialist hospital for cochlear implant were analyzed. Patients were divided into subgroups based on degree of consanguinity.
The relative risk of having more than one child with SNHL in offspring of a consanguineous marriage.
189 parents and children with CHL.
The parents of 157 children (83.1%) were blood-related. Of those, 48 had more than one child with CHL (31.4%), while only two parents who were not blood-related had more than one child with CHL (6.25%;
=.005). Among the 189 children, 131 (69.3%) parents were direct cousins. Only 39 (20.6%) and 43 (22.8%) children had family histories of CHL on the paternal and maternal sides, respectively. There was no statistically significant difference in the prevalence of auditory neuropathy between the offspring of consanguineous and non-consanguineous marriages (
=.648).
The risk of having more than one child with SNHL in the offspring from a consanguineous marriage is 3.5 times higher than that of a non-consanguineous mating.
The association of hearing loss degree with consanguinity was not studied.
None.</abstract><cop>Saudi Arabia</cop><pub>King Faisal Specialist Hospital and Research Centre</pub><pmid>33307738</pmid><doi>10.5144/0256-4947.2020.456</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-8497-8326</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Child Child, Preschool Consanguinity Cross-Sectional Studies Deafness - epidemiology Deafness - genetics Female Hearing Loss, Sensorineural - congenital Humans Male Marriage - ethnology Middle East - epidemiology Original Pedigree Risk Factors |
title | The association between consanguineous marriage and offspring with congenital hearing loss |
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