{"title":"同卵双生子一般不一致的先天性甲状腺功能减退症从甲状腺发育不良。","authors":"Guy van Vliet, Gilbert Vassart","doi":"10.1159/000245935","DOIUrl":null,"url":null,"abstract":"In this context, we read with great interest the report by Kuehnen et al. [2] of two pairs of monozygotic twins who are discordant for hypothyroidism due to thyroid dysgenesis. Their report confirms the results of a systematic survey of the Québec and Brussels neonatal screening databases which, together with a review of all published cases since screening began, showed that 12 of the 13 reported pairs (92%) were discordant [3] . Two percent of cases of congenital hypothyroidism from thyroid dysgenesis (CHTD) have an affected relative. This figure is 15-fold higher than what would be predicted by chance alone and clearly suggests a genetic mechanism in those cases [1] . However, it should not be construed as evidence that there is a genetic component in all patients with CHTD, i.e. the 2% with a positive family history and the 98% without may be two discrete populations. Received: June 10, 2009 Accepted: June 24, 2009 Published online: October 19, 2009","PeriodicalId":13225,"journal":{"name":"Hormone research","volume":"72 5","pages":"320"},"PeriodicalIF":0.0000,"publicationDate":"2009-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000245935","citationCount":"8","resultStr":"{\"title\":\"Monozygotic twins are generally discordant for congenital hypothyroidism from thyroid dysgenesis.\",\"authors\":\"Guy van Vliet, Gilbert Vassart\",\"doi\":\"10.1159/000245935\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this context, we read with great interest the report by Kuehnen et al. [2] of two pairs of monozygotic twins who are discordant for hypothyroidism due to thyroid dysgenesis. Their report confirms the results of a systematic survey of the Québec and Brussels neonatal screening databases which, together with a review of all published cases since screening began, showed that 12 of the 13 reported pairs (92%) were discordant [3] . Two percent of cases of congenital hypothyroidism from thyroid dysgenesis (CHTD) have an affected relative. This figure is 15-fold higher than what would be predicted by chance alone and clearly suggests a genetic mechanism in those cases [1] . However, it should not be construed as evidence that there is a genetic component in all patients with CHTD, i.e. the 2% with a positive family history and the 98% without may be two discrete populations. Received: June 10, 2009 Accepted: June 24, 2009 Published online: October 19, 2009\",\"PeriodicalId\":13225,\"journal\":{\"name\":\"Hormone research\",\"volume\":\"72 5\",\"pages\":\"320\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1159/000245935\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Hormone research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1159/000245935\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2009/10/19 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hormone research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000245935","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2009/10/19 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
Monozygotic twins are generally discordant for congenital hypothyroidism from thyroid dysgenesis.
In this context, we read with great interest the report by Kuehnen et al. [2] of two pairs of monozygotic twins who are discordant for hypothyroidism due to thyroid dysgenesis. Their report confirms the results of a systematic survey of the Québec and Brussels neonatal screening databases which, together with a review of all published cases since screening began, showed that 12 of the 13 reported pairs (92%) were discordant [3] . Two percent of cases of congenital hypothyroidism from thyroid dysgenesis (CHTD) have an affected relative. This figure is 15-fold higher than what would be predicted by chance alone and clearly suggests a genetic mechanism in those cases [1] . However, it should not be construed as evidence that there is a genetic component in all patients with CHTD, i.e. the 2% with a positive family history and the 98% without may be two discrete populations. Received: June 10, 2009 Accepted: June 24, 2009 Published online: October 19, 2009