First Page | Document Content | |
---|---|---|
Date: 2013-04-23 17:35:32Health 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.pubAdd to Reading ListSource URL: www.rarediseasesnetwork.orgDownload Document from Source WebsiteFile Size: 1,18 MBShare Document on Facebook |
TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhDDocID: 12v8A - View Document | |
Volume 6, Issue 1 April 2011 State of Tennessee Department of HealthDocID: Jss2 - View Document | |
UCDC Newsletter_4.22.13_Final.pubDocID: HWNL - View Document | |
Volume 6, Issue 1 April 2011 State of Tennessee Department of HealthDocID: 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 overloDocID: BM9n - View Document |