Studying mitochondrial disorders, which result from mitochondrial dysfunction, can reveal critical information about the genetic basis of these conditions. By focusing on the genomics aspects of mitochondrial disorders, researchers can work towards early detection, prevention, and personalized treatment strategies. Genet provides an array of services to support the investigation of genetic factors contributing to mitochondrial disorders, promoting advancements in diagnosis, management, and treatment.
Genetic Disease Research
Digestive System Diseases
Digestive system diseases involve conditions that affect the gastrointestinal tract and related organs. By exploring the genetic and genomic aspects of these diseases, researchers can uncover the underlying genetic factors that contribute to disease onset […]
Genetic Disease Research
Recommended Newborn Screening Panels
Newborn screening panels aim to identify genetic disorders early in life , allowing for timely intervention and improved health outcomes. The use of genomics in newborn screening can facilitate the detection of a broad range […]
Genetic Disease Research
Skin and Connective Tissue Diseases
Understanding the genetic components of skin and connective tissue diseases can offer insights into the development and progression of these conditions affecting the skin, muscles, tendons, and ligaments. Genomic research can aid in early detection […]