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 | Add to Reading List |
![]() | 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 |