Lysosomal Storage Diseases Therapeutics Are Getting Better With Continuous R&D Activities Among Key Pharmaceutical Companies coherentmarketblog.blogspot.com

Lysosomal Storage Disease is a medical condition where proteins, usually DNA, become deformed or lose their catalytic ability. The human genetic material, which is called DNA, is a highly dynamic and sophisticated part of our system. Due to a process called mutations, DNA becomes altered and either changes its directions or becomes a different size. In either case, the genetic information is then unreadable by cells known as enzymes. There are various types of lysosomal storage diseases including Gaucher disease, Fabry disease, Pompe disease, Niemann-Pick disease, Tay-Sachs disease, etc.