What is another word for Deficiency Argininosuccinic Acid Synthetase Complete?
Pronunciation: [dɪfˈɪʃənsi ˌɑːd͡ʒɪnˌɪnəsəksˈɪnɪk ˈasɪd sˈɪnθɪtˌe͡ɪs kəmplˈiːt] (IPA) 
Deficiency Argininosuccinic Acid Synthetase Complete, commonly known as ASL deficiency, is a rare genetic disorder that affects the body's ability to break down the amino acid argininosuccinic acid. Individuals with this condition lack the enzyme argininosuccinic acid synthetase, which is responsible for the production of argininosuccinic acid.
Synonyms for ASL deficiency include argininosuccinate synthetase deficiency, argininosuccinate lyase deficiency, and citrullinemia type 1. These terms can be used interchangeably to refer to the same genetic disorder.
ASL deficiency poses significant health risks, including high ammonia levels in the blood, liver damage, and neurological problems. Early diagnosis and treatment are crucial to managing the condition and preventing complications. Treatment often includes a restricted protein diet, medications to lower ammonia levels, and liver transplantation in severe cases.
