What is another word for Brain Diseases Metabolic Inborn?
Pronunciation: [bɹˈe͡ɪn dɪzˈiːzɪz mˌɛtəbˈɒlɪk ˈɪnbɔːn] (IPA) 
Brain diseases metabolic inborn, also known as inborn errors of metabolism, are a group of rare genetic disorders that affect the body's ability to process certain nutrients. These disorders are caused by defects in specific enzymes or proteins that are involved in metabolism. Although they are individually rare, collectively over 1,000 different inborn errors of metabolism have been identified. Some common examples include phenylketonuria (PKU), maple syrup urine disease (MSUD), and Gaucher's disease. These conditions can lead to a variety of symptoms, ranging from mild to severe, and typically require specialized medical treatment and lifelong management. Detecting and treating these brain diseases metabolic inborn early is crucial in order to prevent long-term complications.
