Mystery Of How Mitochondrial Disease Passes From Mother To Child
Once considered rare, mitochondrial diseases are now thought to affect as many as one person in 5,000. New research in this area hopes to open up more opportunities for predicting a child's risk of developing a mitochondrial disease which can cause muscle weakness, diabetes, strokes, heart failure and epilepsy. All human and animal cells contain many mitochondria, which are involved in energy production within the body. Mitochondria have their own genetic information, known as mitochondrial DNA, or mtDNA, which is inherited. A child only inherits one copy of DNA from each parent but may inherit many copies of mtDNA, which are only passed down from the mother. Scientists have shown for the first time how this particular family of diseases are passed down from mother to child and how this can lead to the severity of the disease differing widely. Mutations in mtDNA can affect energy production within cells and therefore lead to disease. However, mitochondrial diseases...