{"title":"唐氏综合征患者颅面形态的评估:一项颅面测量研究","authors":"P. Subbaiah","doi":"10.21013/JAS.V7.N2.P4","DOIUrl":null,"url":null,"abstract":"D own’s syndrome is a disease entity in which the defect in mental development is associated in a unique way with a large number of physical defects. It is a condition resulting from an extra chromosome 21 and thus the condition is also known as Trisomy 21. It is considered one of the most frequent genetic causes of mental retardation. The incidence of Down’s syndrome is estimated to be between 1.6 to 2.5 per 1000 live births and increases with increase in maternal age. 4,59,10 Mongoloids usually exhibit retarded motor and language skills, with an IQ range from extremely low to 45-55. Cephalometry has now been firmly established as the most essential procedure for gaining knowledge of the complexities of dentofacial skeletal pattern. By utilizing cephalometric radiography, whereby description, morphologic outline, measurement and change in growth of the skull can be fairly accurately ascertained, it might be possible to observe some of the subtle The present study is an attempt to determine cephalometrically whether the group of individuals with Down’s syndrome have a distinctive craniofacial phenotype. The growth of the craniofacial area in the presence of the extra chromosome is also examined.","PeriodicalId":14487,"journal":{"name":"IRA-International Journal of Applied Sciences","volume":"66 1","pages":"75-94"},"PeriodicalIF":0.0000,"publicationDate":"2017-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of Craniofacial Morphology in Subjects with Down’s Syndrome: A Cephalometric Study\",\"authors\":\"P. Subbaiah\",\"doi\":\"10.21013/JAS.V7.N2.P4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"D own’s syndrome is a disease entity in which the defect in mental development is associated in a unique way with a large number of physical defects. It is a condition resulting from an extra chromosome 21 and thus the condition is also known as Trisomy 21. It is considered one of the most frequent genetic causes of mental retardation. The incidence of Down’s syndrome is estimated to be between 1.6 to 2.5 per 1000 live births and increases with increase in maternal age. 4,59,10 Mongoloids usually exhibit retarded motor and language skills, with an IQ range from extremely low to 45-55. Cephalometry has now been firmly established as the most essential procedure for gaining knowledge of the complexities of dentofacial skeletal pattern. By utilizing cephalometric radiography, whereby description, morphologic outline, measurement and change in growth of the skull can be fairly accurately ascertained, it might be possible to observe some of the subtle The present study is an attempt to determine cephalometrically whether the group of individuals with Down’s syndrome have a distinctive craniofacial phenotype. The growth of the craniofacial area in the presence of the extra chromosome is also examined.\",\"PeriodicalId\":14487,\"journal\":{\"name\":\"IRA-International Journal of Applied Sciences\",\"volume\":\"66 1\",\"pages\":\"75-94\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-05-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IRA-International Journal of Applied Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21013/JAS.V7.N2.P4\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IRA-International Journal of Applied Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21013/JAS.V7.N2.P4","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
D own 's综合征是一种疾病实体,其中智力发育缺陷以一种独特的方式与大量身体缺陷联系在一起。这是一种由额外的21号染色体引起的疾病,因此这种疾病也被称为21三体。它被认为是智力迟钝最常见的遗传原因之一。唐氏综合症的发病率估计为每1000例活产1.6至2.5例,并随着产妇年龄的增加而增加。4,59,10蒙古人通常表现为运动和语言技能迟钝,智商范围从极低到45-55。头测术现已被确立为了解牙面骨结构复杂性的最基本的方法。通过使用头颅x线摄影,可以相当准确地确定颅骨的描述、形态轮廓、测量和生长变化,有可能观察到一些微妙的变化。本研究试图通过头颅x线摄影确定唐氏综合征患者群体是否具有独特的颅面表型。在额外染色体存在的情况下,颅面区域的生长也被检查。
Evaluation of Craniofacial Morphology in Subjects with Down’s Syndrome: A Cephalometric Study
D own’s syndrome is a disease entity in which the defect in mental development is associated in a unique way with a large number of physical defects. It is a condition resulting from an extra chromosome 21 and thus the condition is also known as Trisomy 21. It is considered one of the most frequent genetic causes of mental retardation. The incidence of Down’s syndrome is estimated to be between 1.6 to 2.5 per 1000 live births and increases with increase in maternal age. 4,59,10 Mongoloids usually exhibit retarded motor and language skills, with an IQ range from extremely low to 45-55. Cephalometry has now been firmly established as the most essential procedure for gaining knowledge of the complexities of dentofacial skeletal pattern. By utilizing cephalometric radiography, whereby description, morphologic outline, measurement and change in growth of the skull can be fairly accurately ascertained, it might be possible to observe some of the subtle The present study is an attempt to determine cephalometrically whether the group of individuals with Down’s syndrome have a distinctive craniofacial phenotype. The growth of the craniofacial area in the presence of the extra chromosome is also examined.