{"title":"双裂舌病例系列：作为一个孤立的实体","authors":"Ramraj Yadav, Arpit Goyal, S. Saroj, Deepak Kumar Gupta, Vishwambhar Singh, Rajesh Kumar","doi":"10.36106/gjra/9607722","DOIUrl":null,"url":null,"abstract":"Period of organogenesis is very precise duration, any factor affecting this period leads to congenital\nanomaly. Bid tongue is one of the congenital anomalies mostly associated with syndromic cases like\nOpitz G/BBB syndrome, oral–facial– digital syndrome type I, but isolated bid tongue can also be seen rarely. Here we describe\nthree cases of isolated bid tongue in absence of any intra oral or facial defect.","PeriodicalId":12664,"journal":{"name":"Global journal for research analysis","volume":"34 10","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CASE SERIES OF BIFID TONGUE: AS AN ISOLATED ENTITY\",\"authors\":\"Ramraj Yadav, Arpit Goyal, S. Saroj, Deepak Kumar Gupta, Vishwambhar Singh, Rajesh Kumar\",\"doi\":\"10.36106/gjra/9607722\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Period of organogenesis is very precise duration, any factor affecting this period leads to congenital\\nanomaly. Bid tongue is one of the congenital anomalies mostly associated with syndromic cases like\\nOpitz G/BBB syndrome, oral–facial– digital syndrome type I, but isolated bid tongue can also be seen rarely. Here we describe\\nthree cases of isolated bid tongue in absence of any intra oral or facial defect.\",\"PeriodicalId\":12664,\"journal\":{\"name\":\"Global journal for research analysis\",\"volume\":\"34 10\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-02-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Global journal for research analysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36106/gjra/9607722\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Global journal for research analysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36106/gjra/9607722","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
器官形成期是一个非常精确的时期，任何影响这个时期的因素都会导致先天性畸形。双d 舌是先天性畸形之一，多见于综合征病例，如奥皮茨 G/BBB 综合征、口腔-面部-数字综合征 I 型，但孤立的双d 舌也很少见。在此，我们描述了三例在没有任何口腔内或面部缺陷的情况下出现的孤立双d 舌。
CASE SERIES OF BIFID TONGUE: AS AN ISOLATED ENTITY
Period of organogenesis is very precise duration, any factor affecting this period leads to congenital
anomaly. Bid tongue is one of the congenital anomalies mostly associated with syndromic cases like
Opitz G/BBB syndrome, oral–facial– digital syndrome type I, but isolated bid tongue can also be seen rarely. Here we describe
three cases of isolated bid tongue in absence of any intra oral or facial defect.
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