Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Pyruvate carboxylase deficiency disease
Pyruvate carboxylase deficiency, infantile form
Infantile pyruvate carboxylase (PC) deficiency (Type A) is a rare, severe form of PC deficiency characterized by infantile-onset, mild to moderate lactic acidemia, and a generally severe course.
This condition has no sub-types.