What is another word for Combined Carboxylase Deficiency?
Pronunciation: [kəmbˈa͡ɪnd kˈɑːbəksˌɪle͡ɪs dɪfˈɪʃənsi] (IPA) 
Combined Carboxylase Deficiency, also known as multiple carboxylase deficiency, is a rare inherited metabolic disorder that affects the body's ability to break down certain proteins, fats, and carbohydrates. This condition can lead to a range of symptoms including poor feeding, developmental delays, seizures, and metabolic acidosis. Synonyms for Combined Carboxylase Deficiency include multiple carboxylase deficiency syndrome and carboxylase deficiency syndrome. These terms are used interchangeably to describe this specific metabolic disorder characterized by reduced activity of enzymes that are involved in various biochemical reactions. It is important for healthcare professionals and families to be aware of these synonyms to ensure accurate diagnosis and appropriate management for affected individuals.
