Genetics Newborn Screening ProgramState of CT Genetics Newborn Screening Program Health Care Provider Fact Sheet Argininemia or Arginase deficiency Introduction – Urea

QUESTIONS HEALTH CARE PROVIDERS FREQUENTLY ASK REGARDING NEWBORN SCREENINGArgininosuccinic Aciduria (ASA) Description: Argininosuccinic Aciduria (ASA) is one of the urea

Argininosuccinic AcidemiaArgininosuccinic acidemia is a urea cycle disorder in which the argininosuccinic acid lyase (ASAL) enzyme deficiency causes severe hyperammonemia.

Argininosuccinate Lyase Deficiency- JC Edit (1)University of Oklahoma College of Medicine, Oklahoma City, Oklahoma CASE DESCRIPTIONINTRODUCTION Argininosuccinate Lyase (ASL)

18_1.tifJ. Inher. Metab. Dis. 8 (1985) 18 20 Prospective Prevention of Neonatal Hyperammonaemia in Argininosuccinic Acidura by Arginine Therapy S. M. DONN 1 and J. G. THOENE

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