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  2. Argininosuccinic aciduria - Wikipedia

    en.wikipedia.org/wiki/Argininosuccinic_aciduria

    In argininosuccinic aciduria, the enzyme argininosuccinate lyase, involved in the conversion of arginino succinate to arginine within the urea cycle, is damaged or missing. The urea cycle cannot proceed normally, and nitrogen accumulates in the bloodstream in the form of ammonia.

  3. Argininosuccinate lyase - Wikipedia

    en.wikipedia.org/wiki/Argininosuccinate_lyase

    Argininosuccinate lyase is an intermediate enzyme in the urea synthesis pathway and its function is imperative to the continuation of the cycle. A non-functioning enzyme results in patients' accumulation of ammonia, argininosuccinate, and citrulline in the blood, and argininosuccinate is excreted in the urine. [ 9 ]

  4. Adenylosuccinate lyase deficiency - Wikipedia

    en.wikipedia.org/wiki/Adenylosuccinate_lyase...

    Adenylosuccinate lyase deficiency is responsible for a range of symptoms that involve psychomotor retardation, often accompanied by epileptic seizures, and autistic features. Two common theories were proposed to account for these effects, the first is that they result from decreased concentrations of purine nucleotides needed for purine ...

  5. Argininosuccinate synthase - Wikipedia

    en.wikipedia.org/wiki/Argininosuccinate_synthase

    Argininosuccinate synthase or synthetase (ASS; EC 6.3.4.5) is an enzyme that catalyzes the synthesis of argininosuccinate from citrulline and aspartate.In humans, argininosuccinate synthase is encoded by the ASS gene located on chromosome 9.

  6. Adenylosuccinate lyase - Wikipedia

    en.wikipedia.org/wiki/Adenylosuccinate_lyase

    Mutated adenylosuccinate lyase (ASL) causes clinical disease in patients that is referred to as adenylosuccinate lyase deficiency. This condition is rare, and it presents with varying degrees of psychomotor retardation , autism , muscle wasting , and epilepsy .

  7. Isolated 17,20-lyase deficiency - Wikipedia

    en.wikipedia.org/.../Isolated_17,20-lyase_deficiency

    The symptoms of isolated 17,20-lyase deficiency, in males, include pseudohermaphroditism (i.e., feminized, ambiguous, or mildly underdeveloped (e.g., micropenis, perineal hypospadias, and/or cryptorchidism (undescended testes)) external genitalia), female gender identity, and, in non-complete cases of deficiency where partial virilization occurs, gynecomastia up to Tanner stage V (due to low ...

  8. More Than Half of People with Diabetes Are Deficient in This ...

    www.aol.com/lifestyle/more-half-people-diabetes...

    Magnesium ranked second as the most common deficiency, with about 42% of people with type 2 diabetes deficient in magnesium. In a subgroup of people with diabetes taking metformin, a common ...

  9. Argininosuccinic acid - Wikipedia

    en.wikipedia.org/wiki/Argininosuccinic_acid

    Argininosuccinic acid is a precursor to fumarate in the citric acid cycle via argininosuccinate lyase. [5] See also. Succinic acid; References