| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10833627 | Molecular Genetics and Metabolism | 2014 | 9 Pages |
Abstract
This study is the largest reported follow-up of infants with NBS screen-positive results for suspected VLCADD and demonstrates the necessity of developing comprehensive and consistent long-term follow-up NBS systems. Application of clinical information revealed differences between symptomatic and asymptomatic children with VLCADD. Comparison of NBS analytes and analyte ratios may be valuable in developing more effective diagnostic algorithms.
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Authors
J. Lawrence II, Sverre Vedal, Jose E. Abdenur, Sylvia M. Au, Bruce A. Barshop, Lisa Feuchtbaum, Cary O. Harding, Cheryl Hermerath, Fred Lorey, David E. Sesser, John D. Thompson, Arthur Yu,