What is another word for PDHC Deficiency Diseases?
Pronunciation: [pˌiːdˌiːˌe͡ɪt͡ʃsˈiː dɪfˈɪʃənsi dɪzˈiːzɪz] (IPA) 
PDHC deficiency diseases, also known as pyruvate dehydrogenase complex deficiency diseases, refer to a group of rare genetic disorders. These conditions result from a deficiency or dysfunction in the pyruvate dehydrogenase complex, an enzyme crucial for the energy production process in our cells. To describe these conditions, several synonyms can be used. They include Pyruvate Dehydrogenase Deficiency, PDH Deficiency, and Pyruvate Dehydrogenase Complex Deficiency. Furthermore, they might be referred to as Pyruvate Dehydrogenase E1-alpha Deficiency, Pyruvate Dehydrogenase E1-beta Deficiency, or even Pyruvate Dehydrogenase E3-binding Protein Deficiency, depending on the specific enzyme deficiency involved. These diseases manifest in various ways, affecting an individual's neurological development, metabolism, and overall health.
