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What is another word for Argininosuccinic Acid Synthetase Deficiency Disease?

Pronunciation: [ˌɑːd͡ʒɪnˌɪnəsəksˈɪnɪk ˈasɪd sˈɪnθɪtˌe͡ɪs dɪfˈɪʃənsi dɪzˈiːz] (IPA)

Argininosuccinic Acid Synthetase Deficiency Disease, also known as Argininosuccinic Aciduria or Citrullinemia type 1, is a rare genetic disorder that affects the urea cycle. This condition occurs when there is a deficiency of the enzyme argininosuccinic acid synthetase, leading to the accumulation of toxic levels of ammonia in the body. Individuals with this disease may experience developmental delay, intellectual disability, seizures, and liver damage. Synonyms for this condition include ASSD deficiency, Argininosuccinic Acid Synthetase Deficiency, and Argininosuccinic Acid Synthetase Deficiency Syndrome. These terms are used interchangeably to describe the same rare genetic disorder. Early diagnosis and treatment are crucial to managing symptoms and preventing complications associated with this condition.
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What are the opposite words for Argininosuccinic Acid Synthetase Deficiency Disease?

Antonyms are words that have opposite meanings. Unfortunately, there are no antonyms for the long scientific term "Argininosuccinic Acid Synthetase Deficiency Disease." The medical condition, also known as citrullinemia type I (CTLN1), is a rare genetic disorder that affects the urea cycle, leading to a buildup of toxic ammonia in the body. While there may not be antonyms for this disease, there are treatments available such as a low-protein diet, medications, and a liver transplant in severe cases. Early diagnosis and treatment can help individuals with this condition live a full and healthy life.

What are the antonyms for Argininosuccinic acid synthetase deficiency disease?

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