Congenital Lactic Acidosis (CLA) is a rare metabolic disorder characterized by the inability of the body to break down lactate. This leads to the accumulation of lactic acid in the blood and tissues, resulting in various symptoms such as muscle weakness, developmental delay, and seizures. CLA is caused by genetic mutations in the genes involved in the lactate metabolism pathway.
No Results Found
Sorry, there are no results for this search. Please try searching by condition, treatment or keyword