Publication Type : Journal Article
Thematic Areas : Medical Sciences
Publisher : Genetic Disorders Genetic Reports
Source : Genetic Disorders & Genetic Reports, SciTechnol, Volume 2014 (2015)
Url : https://www.scitechnol.com/molecular-genetic-testing-prenatal-diagnosis-computational-oculocutaneous-albinism-type-BseJ.php?article_id=2014
Campus : Kochi
School : School of Medicine
Department : Paediatrics
Verified : Yes
Year : 2015
Abstract : In India epidemiological-communicable diseases are on the decline due to better living conditions and healthcare delivery in the society. On the other hand, the relative increase in the prevalence of genetic diseases threatens to be a public health problem. One such group of metabolic disorder is Albinism. General population based oculocutaneous albinism (OCA) carrier screening is controversial in all the races. Because of the occurrence of this disease in prior generations, it is necessary to create the knowledge, so that even uneducated affected family members will be willing to diagnose the disease status. As a result, the carrier detection in general population has become necessary in Indian population.
Cite this Research Publication : K. Renugadevi, Mary, J. Asnet, Perumalsamy, V., Seshadri, S., Jagadeesh, S., Suresh, B., Dr. Sheela Nampoothiri, Shenbagarathai, R., Krishnaswamy, S., and Sundaresan, P., “Molecular Genetic Testing for Carrier-Prenatal Diagnosis and Computational Analysis of Oculocutaneous Albinism Type 1”, Genetic Disorders & Genetic Reports, vol. 2014, 2015.