Aram Kim, Stacey Rogers, Jennifer Archibald, Neeta Chandwani
{"title":"兄弟姐妹GAPO综合征的牙科治疗。","authors":"Aram Kim, Stacey Rogers, Jennifer Archibald, Neeta Chandwani","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>GAPO syndrome is a rare autosomal recessive genetic disorder, characterized by growth retardation, alopecia, pseudoanodontia, and progressive ocular changes. This disorder is caused by recessive mutations in the ANTXR1 gene and has characteristic dysmorphic facial features along with connective tissue changes, cardiomyopathy, gonadal dysfunction and craniosynostosis. The most common dental implication of GAPO syndrome is pseudoanodontia caused by eruption failure of the primary and permanent dentition. Currently, there is no standard treatment for patients with GAPO syndrome. Management often includes multidisciplinary care in the surveillance of syndromic sequelae and supportive treatment of symptomatic health concerns, which are unique to each patient. The purpose of this paper is to describe the dental rehabilitation of two brothers with GAPO syndrome.</p>","PeriodicalId":51605,"journal":{"name":"JOURNAL OF DENTISTRY FOR CHILDREN","volume":"88 2","pages":"134-139"},"PeriodicalIF":0.4000,"publicationDate":"2021-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dental Management of Siblings with GAPO Syndrome.\",\"authors\":\"Aram Kim, Stacey Rogers, Jennifer Archibald, Neeta Chandwani\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>GAPO syndrome is a rare autosomal recessive genetic disorder, characterized by growth retardation, alopecia, pseudoanodontia, and progressive ocular changes. This disorder is caused by recessive mutations in the ANTXR1 gene and has characteristic dysmorphic facial features along with connective tissue changes, cardiomyopathy, gonadal dysfunction and craniosynostosis. The most common dental implication of GAPO syndrome is pseudoanodontia caused by eruption failure of the primary and permanent dentition. Currently, there is no standard treatment for patients with GAPO syndrome. Management often includes multidisciplinary care in the surveillance of syndromic sequelae and supportive treatment of symptomatic health concerns, which are unique to each patient. The purpose of this paper is to describe the dental rehabilitation of two brothers with GAPO syndrome.</p>\",\"PeriodicalId\":51605,\"journal\":{\"name\":\"JOURNAL OF DENTISTRY FOR CHILDREN\",\"volume\":\"88 2\",\"pages\":\"134-139\"},\"PeriodicalIF\":0.4000,\"publicationDate\":\"2021-05-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JOURNAL OF DENTISTRY FOR CHILDREN\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JOURNAL OF DENTISTRY FOR CHILDREN","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
GAPO syndrome is a rare autosomal recessive genetic disorder, characterized by growth retardation, alopecia, pseudoanodontia, and progressive ocular changes. This disorder is caused by recessive mutations in the ANTXR1 gene and has characteristic dysmorphic facial features along with connective tissue changes, cardiomyopathy, gonadal dysfunction and craniosynostosis. The most common dental implication of GAPO syndrome is pseudoanodontia caused by eruption failure of the primary and permanent dentition. Currently, there is no standard treatment for patients with GAPO syndrome. Management often includes multidisciplinary care in the surveillance of syndromic sequelae and supportive treatment of symptomatic health concerns, which are unique to each patient. The purpose of this paper is to describe the dental rehabilitation of two brothers with GAPO syndrome.
期刊介绍:
Acquired after the merger between the American Society of Dentistry for Children and the American Academy of Pediatric Dentistry in 2002, the Journal of Dentistry for Children (JDC) is an internationally renowned journal whose publishing dates back to 1934. Published three times a year, JDC promotes the practice, education and research specifically related to the specialty of pediatric dentistry. It covers a wide range of topics related to the clinical care of children, from clinical techniques of daily importance to the practitioner, to studies on child behavior and growth and development. JDC also provides information on the physical, psychological and emotional conditions of children as they relate to and affect their dental health.