POLG diseases: Rare genetic conditions that starve cells of energy

Sly Saint · Mar 13, 2025

Disease name: Polymerase gamma-related diseases, called POLG-related diseases for short

Affected populations: POLG-related diseases are a group of rare, incurable conditions caused by inherited gene mutations. These disease-causing mutations are carried by up to 2% of people of Northern European descent. However, not everyone who carries the mutations ultimately develops a POLG-related disorder.

Estimates suggest that these diseases affect approximately 1 in 10,000 people worldwide.

Causes: POLG-related diseases are caused by several hundred different mutations in the POLG gene. This gene encodes a protein in mitochondria, called DNA polymerase gamma (pol γ), which is needed to replicate and repair the unique DNA found only inside mitochondria, rather than in the cell nucleus.

People develop POLG-related diseases by inheriting either one or two copies of the mutated POLG gene from one or both of their parents.

Mitochondria are the cellular powerhouses responsible for breaking down the carbohydrates and fatty acids in food to produce molecules called ATP, which the body then uses as energy.

In people with POLG-related diseases, issues with polymerase gamma can either end up decreasing the amount of DNA in mitochondria or introducing mutations into that DNA. And in some cases, both these events can occur.
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POLG diseases: Rare genetic conditions that starve cells of energy and afflicted the late Prince of Luxembourg

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POLG diseases: Rare genetic conditions that starve cells of energy

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