UCDC Newsletter_4.22.13_Final.pub

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Date: 2013-04-23 17:35:32 Health Urea cycle disorder Ornithine transcarbamylase deficiency Argininosuccinic aciduria Hyperammonemia Ornithine translocase deficiency Arginase Citrullinemia N-Acetylglutamate synthase deficiency Urea cycle Metabolism Biology		UCDC Newsletter_4.22.13_Final.pub Add to Reading List Source URL: www.rarediseasesnetwork.org Download Document from Source Website File Size: 1,18 MB 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
	UCDC Newsletter_4.22.13_Final.pub DocID: HWNL - View Document
	AMINO ACID DISORDERS Karla J Matteson, PhD, FACMG University of Tennessee Genetic Center, Knoxville Outcome without screening: The amino acid disorders are a collection of disorders that involve enzyme deficiencies that DocID: HMYb - View Document
	Citrullinemia (CIT) (metabolic condition: amino acid disorder) Also known as: • citrullinuria DocID: Ehty - View Document
	NEWBORN SCREENING FACT SHEET ASAS Deficiency (Citrullinemia) also milder forms that start later in infancy or childhood. There is also a rare adult form more common in people of Japanese heritage. DocID: zHqm - View Document