Mitochondrial Clinic

Conditions We Treat

We evaluate and treat children with mitochondrial disease such as these: 

• Acyl-CoA dehydrogenase 9 (ACAD9) deficiency
• Barth Syndrome
• Combined oxidative phosphorylation deficiency syndromes
• Leigh syndrome
• Leber hereditary optic neuropathy (LHON)
• Large scale single mitochondrial DNA deletion syndrome (e.g., Kearns-Sayre syndrome)
• Mitochondrial DNA depletion syndromes (e.g., POLG-related mitochondrial disorder)
• Mitochondrial encephalomyopathy, lactic acidosis, with stroke-like episodes (MELAS)
• Myoclonic epilepsy with ragged-red fibers (MERRF) 
• Primary coenzyme Q10 deficiency 
• Pyruvate dehydrogenase complex deficiency (PDH)