Ornithine transcarbamylase - Document - PDFSEARCH.IO

First Page		Document Content
Date: 2003-12-03 18:40:58 Health Urea cycle disorder Argininosuccinate synthase Citrullinemia N-Acetylglutamate synthase deficiency Hyperammonemia Ornithine transcarbamylase deficiency Argininosuccinic aciduria Argininemia Urea cycle Metabolism Biology		Add to Reading List Source URL: rarediseasesnetwork.epi.usf.edu Download Document from Source Website File Size: 100,53 KB Share Document on Facebook

	TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD DocID: 12v8A - View Document
	Volume 6, Issue 1 April 2011 State of Tennessee Department of Health DocID: Jss2 - View Document
	UCDC Newsletter_4.22.13_Final.pub DocID: HWNL - View Document
	Volume 6, Issue 1 April 2011 State of Tennessee Department of Health DocID: Heit - View Document
	Diagnosis: Argininosuccinic Aciduria or Arginosuccinic Lyase Deficiency (ASA) ASA is an inherited disorder that limits the body’s ability to convert ammonia to urea. During periods of illness, fasting or protein overlo DocID: BM9n - View Document