{"title":"Genetic Testing of Huntington’s Disease by Facial Examination of a Mankind using AI Programs","authors":"S. Feroze, S. Nasim","doi":"10.1109/ICONICS56716.2022.10100480","DOIUrl":null,"url":null,"abstract":"This Genetic disorder is considered as one of the major challenges faced by Medical Sciences as it is inherited by humans from one generation to another. With an increasing number of natives of the World at a higher rate, it causes a major impact on information society socially and economically during their lifetime. The citizens of Pakistan and Indian sub continents are facing genomic disease in probably high frequency as compared to other continents. Occurrence of congenital diseases in Pakistan results in higher percentages of unusual genetic diseases especially in children. After analyzing all the current scenarios, some goals and objectives were settled in order to facilitate and give general awareness to people. The objectives of systematic review are evaluation of diagnostic accuracy of AI for the identification of genome contributions to the pathogenesis of Huntington’s disease through facial probe AI to accurately identify genetic disorders. The narrative review is performed in Ned University. In this proceeding sequence, 30 cases of both Normal and Genetically affected Patients were documented in which some certain sorts of tests were performed by using facial recognition. For this FR test, at first a combo list of information of all six emotions of a human being i.e. (Happy, Sorrow, Amazed, Fear, Anger, Revulsion) is gathered in the form of mutated images, which was then later be arranged into a pseudo-random order. Now with the help of Vision Technology we have applied some CV Techniques for the extraction of large pattern sets of features. Lastly the purpose of ML and DL techniques is to receive and compare those morphed image data from the Facial Database in order to identify each of six different emotions of HD & Normal Person. This whole procedure is conducted in real time. Hence in this way we may recognize the HD genetic disorder among the people in an efficient way. The detailed procedure is explained in the Methodology section of this narrative review. Implementation of this process will bring an amazing accountability in suppressing Genetic testing HD in clinical practice.","PeriodicalId":308731,"journal":{"name":"2022 3rd International Conference on Innovations in Computer Science & Software Engineering (ICONICS)","volume":"10 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2022 3rd International Conference on Innovations in Computer Science & Software Engineering (ICONICS)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ICONICS56716.2022.10100480","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
This Genetic disorder is considered as one of the major challenges faced by Medical Sciences as it is inherited by humans from one generation to another. With an increasing number of natives of the World at a higher rate, it causes a major impact on information society socially and economically during their lifetime. The citizens of Pakistan and Indian sub continents are facing genomic disease in probably high frequency as compared to other continents. Occurrence of congenital diseases in Pakistan results in higher percentages of unusual genetic diseases especially in children. After analyzing all the current scenarios, some goals and objectives were settled in order to facilitate and give general awareness to people. The objectives of systematic review are evaluation of diagnostic accuracy of AI for the identification of genome contributions to the pathogenesis of Huntington’s disease through facial probe AI to accurately identify genetic disorders. The narrative review is performed in Ned University. In this proceeding sequence, 30 cases of both Normal and Genetically affected Patients were documented in which some certain sorts of tests were performed by using facial recognition. For this FR test, at first a combo list of information of all six emotions of a human being i.e. (Happy, Sorrow, Amazed, Fear, Anger, Revulsion) is gathered in the form of mutated images, which was then later be arranged into a pseudo-random order. Now with the help of Vision Technology we have applied some CV Techniques for the extraction of large pattern sets of features. Lastly the purpose of ML and DL techniques is to receive and compare those morphed image data from the Facial Database in order to identify each of six different emotions of HD & Normal Person. This whole procedure is conducted in real time. Hence in this way we may recognize the HD genetic disorder among the people in an efficient way. The detailed procedure is explained in the Methodology section of this narrative review. Implementation of this process will bring an amazing accountability in suppressing Genetic testing HD in clinical practice.