Mitochondrial Diseases, Primary (nuclear DNA-encoded)

Primary mitochondrial diseases (PMDs) are a group of genetic diseases in which the mitochondria in the body's cells do not develop or work properly. Mitochondria are tiny structures in the body where the chemical called ATP, the body's energy source, is made. Mitochondria are in cells throughout the body in organs that have high energy demands, such as the muscles, heart, and brain.

The main source of DNA in the body, called nuclear DNA (nDNA), has instructions for genes and proteins that allow mitochondria to make enough energy for the body. nDNA is passed from both parents to their children. Nuclear DNA-encoded PMDs (nDNA PMDs) are caused by changes (or mutations) in nDNA genes.

Someone may be first thought to have a nDNA PMD by their symptoms and their family medical history. Symptoms can vary from person to person, even in the same family. nDNA PMDs usually progress over time and affect multiple organs in the body. Common symptoms include fatigue, muscle weakness, stroke, vision loss, heart rhythm problems, abnormal digestive system movement, and lactic acidosis (a buildup of lactic acid in the body).

Someone may also be diagnosed with a nDNA PMD by genetic testing that studies their nDNA for mutations. Genetic testing can confirm a diagnosis that is being considered based on a person's symptoms and family medical history.

Within nDNA PMDs are two different groups of mitochondrial disease:

  • Mitochondrial respiratory chain disorders (MRCDs)
  • Mitochondrial myopathies, primary (PMMs)

This content comes from a hidden element on this page.

The inline option preserves bound JavaScript events and changes, and it puts the content back where it came from when it is closed.

Remember Me