CLSI NBS06 A : 1ED 2013
Current
The latest, up-to-date edition.
NEWBORN BLOOD SPOT SCREENING FOR SEVERE COMBINED IMMUNODEFICIENCY BY MEASUREMENT OF T-CELL RECEPTOR EXCISION CIRCLES
Hardcopy , PDF
English
30-04-2013
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Abstract
Committee Membership
Foreword
1 Scope
2 Introduction
3 Standard Precautions
4 Terminology
5 Biology of Severe Combined Immunodeficiency
6 Biological and Clinical Features of Severe
Combined Immunodeficiency
7 Overview of Quantitative Polymerase Chain
Reaction Assays
8 Implementation of T-cell Receptor Excision
Circle Assay
9 Follow-up Activities, Communication, and
Diagnostic Testing
References
Appendix A - Immunodeficiency Disorders and T-cell
Receptor Excision Circle Values in the
Newborn Screening Period
Appendix B - Generic Flow Chart for Assays to Measure T-cell
Receptor Excision Circles in newborn Dried
Blood Spot Specimens
Appendix C - Example Algorithms Used for Severe Combined
Immunodeficiency Newborn Screening Testing
and Follow-up
Appendix D - References Materials for the T-cell Receptor
Excision Circle Assay in Dried Blood Spot
Specimens
Appendix E - Example of a Daily Work Plan for Severe
Combined Immunodeficiency Newborn Screening
The Quality Management System Approach
Related CLSI Reference Materials
Specifies the detection of severe combined immunodeficiency (SCID) by population-based newborn screening using dried blood spot specimens to measure T-cell receptor excision circles.
| DocumentType |
Standard
|
| ISBN |
1-56238-871-1
|
| Pages |
92
|
| PublisherName |
Clinical Laboratory Standards Institute
|
| Status |
Current
|
| CLSI NBS01 A6 : 6ED 2013 | BLOOD COLLECTION ON FILTER PAPER FOR NEWBORN SCREENING PROGRAMS |
| CLSI POCT4 A2 : 2ED 2006 | POINT-OF-CARE IN VITRO DIAGNOSTIC (IVD) TESTING |
| CLSI EP17 A2 : 2ED 2012 | EVALUATION OF DETECTION CAPABILITY FOR CLINICAL LABORATORY MEASUREMENT PROCEDURES |
| CLSI POCT8 A : 1ED 2010 | QUALITY PRACTICES IN NONINSTRUMENTED POINT-OF-CARE TESTING: AN INSTRUCTIONAL MANUAL AND RESOURCES FOR HEALTH CARE WORKERS |
| CLSI I/LA31 P : 1ED 2008 | NEWBORN SCREENING GUIDELINES FOR PREMATURE AND/OR SICK NEWBORNS<br> |
| CLSI EP12 A2 : 2ED 2008 | USER PROTOCOL FOR EVALUATION OF QUALITATIVE TEST PERFORMANCE |
| CLSI GP29 A2 : 2ED 2008 | ASSESSMENT OF LABORATORY TESTS WHEN PROFICIENCY TESTING IS NOT AVAILABLE |
| CLSI M29 A3 : 3ED 2005 | ACQUIRED INFECTIONS; APPROVED GUIDELINE |
| CLSI H42 A2 : 2ED 2007 | ENUMERATION OF IMMUNOLOGICALLY DEFINED CELL POPULATIONS BY FLOW CYTOMETRY |
| CLSI MM1 A3 : 3ED 2012 | MOLECULAR METHODS FOR CLINICAL GENETICS AND ONCOLOGY TESTING |
| CLSI LA4 A4 : 4ED 2003 | BLOOD COLLECTION ON FILTER PAPER FOR NEWBORN SCREENING PROGRAMS |
| CLSI I/LA27 A : 1ED 2006 | NEWBORN SCREENING FOLLOW-UP |
| CLSI QMS02 A6 : 6ED 2013 | QUALITY MANAGEMENT SYSTEM: DEVELOPMENT AND MANAGEMENT OF LABORATORY DOCUMENTS |
| CLSI I/LA26 A : 1ED 2004 | PERFORMANCE OF SINGLE CELL IMMUNE RESPONSE ASSAYS |
| CLSI H26 A2 : 2ED 2010 | VALIDATION, VERIFICATION, AND QUALITY ASSURANCE OF AUTOMATED HEMATOLOGY ANALYZERS |
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