What is another word for Neonatal Pyruvate Dehydrogenase Complex Deficiency Disease?
Pronunciation: [nˈiːə͡ʊnˌe͡ɪtə͡l pˈa͡ɪɹuːvˌe͡ɪt dˌiːha͡ɪdɹˈə͡ʊd͡ʒne͡ɪs kˈɒmplɛks dɪfˈɪʃənsi dɪzˈiːz] (IPA) 
Neonatal Pyruvate Dehydrogenase Complex Deficiency Disease, also known as PDCD, is a rare genetic disorder that affects the body's ability to convert food into energy. This condition is caused by a deficiency of the pyruvate dehydrogenase complex, an enzyme involved in the production of energy in cells. Despite its complex name, there are a few synonymous terms used to refer to this condition. Some alternative names include Neonatal PDH Deficiency, Neonatal Leigh Syndrome, and Pyruvate Dehydrogenase (PDH) Deficiency. Regardless of the terminology used, this disorder can lead to severe neurological symptoms in affected infants, requiring specialized medical management and support.
