What is another word for Amino Acid Metabolism Disorders Inborn?
Pronunciation: [ɐmˈiːnə͡ʊ ˈasɪd mətˈabəlˌɪzəm dɪsˈɔːdəz ˈɪnbɔːn] (IPA) 
Amino acid metabolism disorders inborn, also known as inborn errors of metabolism, are a group of genetic disorders that affect the body's ability to properly metabolize amino acids. These disorders are characterized by a dysfunction in the enzymes responsible for breaking down and processing amino acids. While there are numerous specific amino acid metabolism disorders, they all share common symptoms such as developmental delays, intellectual disabilities, seizures, and even life-threatening complications. Some synonyms for this condition include inborn errors of amino acid metabolism, inherited metabolic disorders, and genetic amino acid disorders. Early diagnosis and management are vital to prevent long-term complications and ensure a healthy quality of life for individuals affected by these disorders.
