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Baby Detect : Genomic Newborn Screening
NCT05687474
- Conditions
- 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
- Locations
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- CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium
NCT05411835
- Conditions
- Carnitine Palmitoyltransferase Deficiency 2, Carnitine palmitoyl transferase 2 deficiency, Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency, +4 more
- Locations
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- Oregon Health & Science University Portland, Oregon, United States
NCT02517307
- Conditions
- Carnitine Palmitoyltransferase II Deficiency, Late-Onset, Carnitine Palmitoyltransferase II Deficiency, Myopathic, Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency, +7 more
- Locations
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- Oregon Health & Science University Portland, Oregon, United States
NCT01494051
- Conditions
- Carnitine Palmitoyltransferase 2 Deficiency, Carnitine palmitoyl transferase 2 deficiency, Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency, +4 more
- Locations
-
Not specified
Active, Not Recruiting
Early Check: Expanded Screening in Newborns
NCT03655223
- Conditions
- 17 Alpha-Hydroxylase Deficiency, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, +456 more
- Locations
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- RTI International Research Triangle Park, North Carolina, United States