{"title":"A Rare Case; Focal Acral Hyperkeratosis","authors":"Neşe GÖÇER GÜROK, Savaş Öztürk, Ahmet Kılıçarslan","doi":"10.17517/ksutfd.1063964","DOIUrl":null,"url":null,"abstract":"Focal acral hyperkeratosis (FAH) is a rare genodermatosis. FAH is usually observed in the second or third decades of life, and it is a type of palmoplantar keratoderma, a heterogeneous group of diseases characterized by abnormal incrassation of the palms and soles. Although it is an autosomal dominant inheritance, it could also be sporadic. It is also known as a rare variant of Costa's Acrokeratoelastoidosis (AKE). Its etiology is not known clearly and there is no effective treatment. In the present study, a 43-year-old recently diagnosed FAH case is presented due to its rarity and frequent confusion with AKE based on current literature","PeriodicalId":34113,"journal":{"name":"Kahramanmaras Sutcu Imam Universitesi Tip Fakultesi dergisi","volume":"15 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kahramanmaras Sutcu Imam Universitesi Tip Fakultesi dergisi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17517/ksutfd.1063964","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
Focal acral hyperkeratosis (FAH) is a rare genodermatosis. FAH is usually observed in the second or third decades of life, and it is a type of palmoplantar keratoderma, a heterogeneous group of diseases characterized by abnormal incrassation of the palms and soles. Although it is an autosomal dominant inheritance, it could also be sporadic. It is also known as a rare variant of Costa's Acrokeratoelastoidosis (AKE). Its etiology is not known clearly and there is no effective treatment. In the present study, a 43-year-old recently diagnosed FAH case is presented due to its rarity and frequent confusion with AKE based on current literature