Dr. Ch. Aparanjitha, Dr. Avinash Tejaswi M. L, Dr. Revathi Rajeshwarkar, Dr. B. Balaji Babu, D. Kavitha, Dr. Archana Pokala, Dr. M. Vishnu Vardhan Reddy
{"title":"Hypohydrotic Ectodermal Dysplasia: A Case Report and Literature Review","authors":"Dr. Ch. Aparanjitha, Dr. Avinash Tejaswi M. L, Dr. Revathi Rajeshwarkar, Dr. B. Balaji Babu, D. Kavitha, Dr. Archana Pokala, Dr. M. Vishnu Vardhan Reddy","doi":"10.36346/sarjods.2022.v04i01.002","DOIUrl":null,"url":null,"abstract":"Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ectoderm of the developing embryo. In the triad of alopecia or hypotrichosis and palmoplantar hyperkeratosis, nail dystrophy is usually accompanied by a lack of sweat glands and a partial or complete absence of primary and/ or permanent dentition. Here, we are presenting a rare case of Ectodermal dysplasia in a 7-year female with classic features of this condition.","PeriodicalId":299258,"journal":{"name":"South Asian Research Journal of Oral and Dental Sciences","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"South Asian Research Journal of Oral and Dental Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36346/sarjods.2022.v04i01.002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ectoderm of the developing embryo. In the triad of alopecia or hypotrichosis and palmoplantar hyperkeratosis, nail dystrophy is usually accompanied by a lack of sweat glands and a partial or complete absence of primary and/ or permanent dentition. Here, we are presenting a rare case of Ectodermal dysplasia in a 7-year female with classic features of this condition.