Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba: 1980-2020
Glutaric aciduria type 1 (GA1) is a severe inherited neurometabolic disorder whose clinical outcome has improved after implementation of newborn screening (NBS) programs and prompt beginning of guideline-directed presymptomatic metabolic treatment. We report the outcome of our 40-year experience wit...
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| Hauptverfasser: | , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
25 November 2020
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| In: |
Molecular genetics and metabolism reports
Year: 2020, Jahrgang: 25, Pages: 1-3 |
| ISSN: | 2214-4269 |
| DOI: | 10.1016/j.ymgmr.2020.100666 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.ymgmr.2020.100666 Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S2214426920301129 |
| Verfasserangaben: | A. Mhanni, N. Aylward, N. Boy, B. Martin, A. Sharma, C. Rockman-Greenberg |
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| 520 | |a Glutaric aciduria type 1 (GA1) is a severe inherited neurometabolic disorder whose clinical outcome has improved after implementation of newborn screening (NBS) programs and prompt beginning of guideline-directed presymptomatic metabolic treatment. We report the outcome of our 40-year experience with the diagnosis and management of GA1 which has improved but remains suboptimal. | ||
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