alanine glyoxylate aminotransferase deficiency

Alanine glyoxylate aminotransferase deficiency is a condition related to plasmalogen biosynthesis. This means that a process in the body that makes important fats called plasmalogens is affected due to a change in the AGXT gene. People with this condition have a mutation in the AGXT gene. This mutation disrupts the normal production of plasmalogens, but further details about the symptoms and overall impact on health are not fully detailed in this summary.

Information about symptoms is currently limited for this condition.

This condition is caused by a mutation in the AGXT gene. The mutation interferes with plasmalogen biosynthesis, which is a key process in the body for producing certain types of fats.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.