An illness characterised by one or more anomalies in the genome is referred to as a genetic condition. It can be brought on by a chromosomal aberration, a mutation in a single gene (monogenic), a number of genes (polygenic), or both. The phrase is typically used when addressing illnesses having a single genetic origin, either in a gene or chromosome, even though polygenic disorders are the most prevalent. De novo mutations occur spontaneously before embryonic development. Autosomal recessive inheritance occurs when two parents carry the same defective gene, or when a parent already has the condition (autosomal dominant inheritance). A genetic ailment is also categorised as a hereditary disease if it is inherited from either one or both parents.
Title : The impact of AI on the future of public health and preventative healthcare
David John Wortley, International Society of Digital Medicine (ISDM), United Kingdom
Title : Personalized and Precision Medicine (PPM) as a unique healthcare model to secure the human healthcare, wellness and biosafety through the view of public health, network-driven healthcare services and lifestyle management
Sergey Suchkov, National Center for Human Photosynthesis, Mexico
Title : Managing integration and interoperability of intelligent and ethical transformed health and social care ecosystems
Habil Bernd Blobel, University of Regensburg, Germany
Title : Study scalp electroacupuncture therapy for autism spectrum disorder
Zhenhuan Liu, University of Chinese Medicine, China
Title : Environmental Public Health Impact Assessment (EHIA) process for tobacco processing plants
Vijayan Gurumurthy Iyer, Techno-Economic- Environmental Study and Check Consultancy Services, India
Title : Therapeutic potential of Benincasa hispida extract in regulating metabolic markers among patients with type 2 diabetes
Wan Rosli Wan Ishak , University Science Malaysia, Malaysia