Genetic Diseases are disorders caused by abnormalities in genes or chromosomes that affect normal growth, development, or body functions. These conditions may be inherited from one or both parents or result from new genetic mutations. Genetic diseases can be classified as single-gene disorders, chromosomal disorders, or multifactorial conditions influenced by both genetic and environmental factors. Common examples include cystic fibrosis, sickle cell anemia, Down syndrome, and muscular dystrophy. Symptoms vary widely depending on the specific disease and may range from mild to severe, affecting physical, intellectual, or metabolic functions. While many genetic diseases have no cure, early diagnosis through genetic testing and newborn screening allows for better management and treatment. Genetic counselling plays a vital role in helping individuals understand risks, make informed decisions, and plan appropriate care. Advances in genetics continue to improve prevention and treatment strategies.
Title : Artificial radionuclides and evolutionary mismatch: Vulnerability of the colon, pancreas, diabetes, and arteries
Sebastiano Venturi, Department of Public Health of Rimini, Italy
Title : Specific strategies over the life course for early identification, prevention, treatment, and long-term support
Christopher Ashton, Center for Recovery, Canada
Title : Population health, public health and the social determinants of health: The state of the science
Adele Ann Webb, Strategic Education, Inc., United States
Title : The nutritional management of healthy menu plans
Iuliana Vintila, Dunărea de Jos University of Galați, Romania
Title : Healthcare system profiles and pandemic outcomes: A cross-country multi-dimensional scaling analysis of Cuba, Spain, Italy, and Germany
Giuseppe Orlando, University of Bari Aldo Moro, Italy
Title : Change your genes – change your life: Epigenetics of longevity
Kenneth R Pelletier, USCF School of Medicine, United States