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What is another word for Late Onset Citrullinemias?

Pronunciation: [lˈe͡ɪt ˈɒnsɛt sˌɪtɹəla͡ɪnˈiːmi͡əz] (IPA)

Late Onset Citrullinemias refer to a group of inherited metabolic disorders characterized by the deficiency of argininosuccinate synthetase (AS). This condition typically manifests later in life, usually during adolescence or adulthood. Several synonyms are used interchangeably to describe this condition, including Adult-Onset Citrullinemia, Late-Onset Citrullinemia, and Type II Citrullinemia. These terms all point to the same disorder with similar clinical features. Patients with Late Onset Citrullinemias often experience recurrent episodes of hyperammonemia, which can lead to life-threatening complications. Prompt diagnosis and management are crucial to minimize the risk of severe ammonia toxicity and improve patient outcomes.
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What are the opposite words for Late Onset Citrullinemias?

Late onset citrullinemias refer to a group of metabolic disorders that affect the body's ability to process the amino acid citrulline. While there are no antonyms for this specific term, it is important to note that there are several conditions that are opposite in nature. For example, early onset citrullinemias present symptoms early in life, while late onset citrullinemias manifest later in life. In addition, conditions that improve or ameliorate the effects of citrullinemias, such as dietary restrictions, medications, or gene therapies, can be considered antonyms in a broader sense. Understanding these opposing concepts can assist doctors and patients in effectively managing the condition.

What are the antonyms for Late onset citrullinemias?

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