Use of Phenylbutyrate Therapy for Patients With Pyruvate Dehydrogenase Complex Deficiency.

Inclusion Criteria: 1. Subject must be older than 3 months old and younger than 18 years old. 2. Clinical diagnosis of PDC deficiency confirmed by DNA testing showing a missense mutation in the PDHA1 gene. 3. Lactate concentration ≥ 2.5 mmol/l or ≥ 2 mmol/l, respectively in venous or arterial blood samples. 4. Provision of signed and dated informed consent form by the parents/legal guardians of the patient 5. Negative pregnancy test for women of childbearing potential, and agree to use effective form of contraception until 6 weeks post treatment. Exclusion Criteria: 1. Frameshift or nonsense mutations of the PDHA1 gene. 2. Defects affecting any gene encoding PDC subunits other than PDHA1 3. Secondary forms of lactic acidosis (e.g. impaired oxygenation or circulation). 4. Tracheostomy or requirement for artificial ventilation. 5. Hyperlactatemia or organic acidosis associated with other metabolic disorders (e.g. biotinidase deficiency, primary disorders of gluconeogenesis, organic acidurias, primary defects of fatty acids oxidation) 6. Evidence of hepatic insufficiency, renal insufficiency, edema with sodium retention, cardiac arrhythmia, congenital heart defects, hypertension, blood dyscrasia, symptomatic pancreatitis, or inflammatory bowel disease. 7. Any clinical condition or medications known to significantly affect renal clearance. 8. Any other condition that, in the opinion of the Investigator, may compromise the safety or compliance of the patient or would preclude the patient from successful completion of the study. 9. Known allergic reactions to components of the study agent. 10. Treatment with another investigational drug or other intervention (including DCA) or participation in a clinical study with an investigational drug within 6 months prior to enrolment. 11. Pregnancy or lactation.