Classification: Inheritance: Population Incidence: Ethnic Incidence: Gene - Argininosuccinate synthase - Document - PDFSEARCH.IO

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Date: 2007-06-25 16:35:48 Chemistry Arginase Argininemia Hyperammonemia Urea cycle disorder Argininosuccinate synthase Ornithine Arginine Urea Urea cycle Metabolism Biology		Classification: Inheritance: Population Incidence: Ethnic Incidence: Gene & Location: Add to Reading List Source URL: www.idph.state.ia.us Download Document from Source Website File Size: 21,24 KB Share Document on Facebook

	STATE of MINNESOTA WHEREAS: Urea Cycle Disorders are rare diseases, occurring at an overall incidence of at least 1 in 35,000 births, and likely higher. Newborns affected with Urea Cycle Disorders can DocID: 19MPN - View Document
	Diagnosis: Argininemia or Arginase Deficiency (ARG) Diagnosis: Argininemia or Arginase Deficiency (ARG) In an emergency, call the Metabolic Specialist immediately. DocID: BEXv - View Document
	NEWBORN SCREENING FACT SHEET ARG 1 Deficiency (Argininemia/Arginase Deficiency) young infants but are not common. Some of the first symptoms of high ammonia are: 1) Poor appetite. DocID: zGcu - View Document
	UREA CYCLE DISORDER GLOSSARY © National Urea Cycle Disorders Foundation 2013 A Allele: One of a pair of genes, situated on the same site on paired chromosomes, containing specific inheritable characteristics. DocID: zdMH - View Document
	Urea cycle disorders A guide for patients, parents and families Contents Introduction ...................................................................................................3 Metabolic function.............. DocID: z5H9 - View Document