At the Medlife assistance we specialize in the diagnosis and treatment of children and adults with inherited metabolic disorders, also known as “inborn errors of metabolism.”
Metabolism refers to all the chemical reactions that take place in our body to break down food to make proteins and other molecules.
Our bodies use these proteins and molecules to function, release energy and convert excess nitrogen into waste products excreted in urine. Metabolic diseases occur when these chemical processes are interrupted, and are often due to enzyme deficiencies caused by errors in single genes. There are hundreds of inherited metabolic diseases. Most people with metabolic diseases begin experiencing symptoms in the newborn period or childhood, but in some, the disease becomes apparent in adulthood.
Many metabolic diseases are treatable. Early diagnosis and treatment may prevent permanent organ damage and death. Treatments vary based on the specific disease and often involve modification of diet and supplementation with specific medications, as well as preemptive inpatient care during infections. Other therapies include enzyme replacement therapy, hematopoietic stem cell transplantation, and organ transplantation.
At Medlife assistance, we evaluate patients with a variety of symptoms, including:
Abnormal newborn screen
Recurrent unexplained illness with dehydration and acidosis
Recurrent hypoglycemia
Altered mental status
Liver disease
Feeding intolerance, recurrent vomiting
Failure to thrive, growth retardation
Developmental delay, intellectual disability
Hypotonia
Progressive deterioration of neurologic function
Epilepsy
Muscle weakness, muscle breakdown
Cardiomyopathy
We diagnose and treat patients who have a wide range of metabolic conditions including:
