Metabolic pathways have pivotal roles in keeping our bodies healthy. Their many actions include producing energy and taking the necessary nutrients from the foods we consume. When a mutation (Genetic Change) occurs in a metabolic pathway, it can lead to either accumulation of toxic substances in our body or insucient production of required products that keep us healthy and functional. As a result, metabolic diseases can affect our health and development, and cause acute and chronic complications.
Evartia Metabolic Test is a
Symptoms of inherited metabolic diseases usually appear shortly after birth. However, depending on the mutation, the metabolic pathway involved and the severity of the condition, some people with inherited metabolic diseases can develop symptoms in early or late adulthood.
Evartia is a new genetic test that detects genetic mutations (changes) that cause inherited metabolic diseases in people.
Evartia metabolic test covers the major categories of inherited metabolic diseases and is offered as a single, detailed panel of 223 genes involved in metabolic pathways.
People with inherited metabolic diseases can have a range of symptoms, with variable expressivity and age of onset. Symptoms can manifest shortly after birth or at infancy, childhood, adolescence or adulthood. Symptoms can also occur suddenly due to specific foods or medications, dehydration, illnesses or other factors. With Evartia, if you have an inherited metabolic disorder, detecting and managing it early can prevent or reduce symptoms, avoid chronic health consequences and improve your quality of life.
Evartia can help you identify: