Newborn screening: Toward a uniform screening panel and system - Executive summary

被引:231
作者
Mann, MY [1 ]
机构
[1] US Hlth Resources & Serv Adm, Genet Serv Branch, Maternal & Child Hlth Bur, Rockville, MD 20857 USA
关键词
D O I
10.1542/peds.2005-26331
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The Maternal and Child Health Bureau commissioned the American College of Medical Genetics to outline a process of standardization of outcomes and guidelines for state newborn screening programs and to define responsibilities for collecting and evaluating outcome data, including a recommended uniform panel of conditions to include in state newborn screening programs. The expert panel identified 29 conditions for which screening should be mandated. An additional 25 conditions were identified because they are part of the differential diagnosis of a condition in the core panel, they are clinically significant and revealed with screening technology but lack an efficacious treatment, or they represent incidental findings for which there is potential clinical significance. The process of identification is described, and recommendations are provided.
引用
收藏
页码:S296 / S307
页数:12
相关论文
共 6 条
  • [1] *CLIN LAB STAND I, 2003, BLOOD COLL FILT PAP
  • [2] MCCABE ERB, 1982, PERINATOL NEONATOL, V6, P63
  • [3] *NAT AC SCI, 1975, GEN SCREEN PROGR PRI
  • [4] Therrell B.L., 1992, SCREEN CORN, V1, P135, DOI DOI 10.1016/0925-6164(92)90005-P
  • [5] Tonniges TF, 2000, PEDIATRICS, V106, P389
  • [6] *US C OFF TECHN AS, 1988, HLTH CHILDR INV FUT, P236