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What is another word for Inborn Amino Acidopathy?

Pronunciation: [ˈɪnbɔːn ɐmˈiːnə͡ʊ ɐsɪdˈɒpəθɪ] (IPA)

Inborn Amino Acidopathy refers to a group of genetic disorders characterized by abnormalities in the metabolism of amino acids. Synonyms for this condition include inborn errors of amino acid metabolism, inborn errors of protein metabolism, or inherited disorders of amino acid metabolism. These disorders result from abnormalities in enzymes responsible for breaking down or converting amino acids. Common examples of inborn amino acidopathies include phenylketonuria (PKU), maple syrup urine disease (MSUD), and homocystinuria. These conditions require careful dietary management to prevent the accumulation of toxic substances in the body. Early diagnosis and treatment play a crucial role in managing these disorders to ensure optimal growth and development of affected individuals.
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What are the opposite words for Inborn Amino Acidopathy?

Inborn amino acidopathy is a rare genetic disorder that affects the metabolism of amino acids. The word inborn suggests that this condition is present from birth, and there are no antonyms that specifically describe a condition that is acquired later in life. However, antonyms for amino acidopathy may include normal amino acid metabolism, amino acid homeostasis, or amino acid balance. These terms describe the opposite of the disrupted metabolism that occurs in individuals with inborn amino acidopathy. It is important to note that there is no cure for this condition, but treatment options may include dietary changes, medication, and other supportive therapies.

What are the antonyms for Inborn amino acidopathy?

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