NCT04602325
- Conditions
- Amino Acid Metabolism, Inborn Errors, Argininosuccinic Aciduria, Brain Diseases, +38 more
- Locations
-
- Children's National Research Institute Washington D.C., District of Columbia, United States
Clinical trial condition
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Explore clinical trials studying Trifunctional Protein Deficiency With Myopathy And Neuropathy. Study availability and eligibility vary by location and protocol.
8 public trials
1 recruiting study
Trifunctional Protein Deficiency With Myopathy And Neuropathy trial results
Completed
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
-
- 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
-
- 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
-
- 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
NCT00654004
- Conditions
- Body Weight, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, +2 more
- Locations
-
- Oregon Health & Science University Portland, Oregon, United States
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
-
- RTI International Research Triangle Park, North Carolina, United States
Active, Not Recruiting
Long-Chain Fatty Acid Oxidation Disorders In-Clinic Disease Monitoring Program
NCT04632953
- Conditions
- Carnitine-Acylcarnitine Translocase Deficiency, Long-chain Fatty Acid Oxidation Disorders (LC-FAOD), Trifunctional Protein Deficiency With Myopathy And Neuropathy, +1 more
- Locations
-
- Phoenix Children's Hospital Phoenix, Arizona, United States
- University of California San Francisco San Francisco, California, United States
- Children's Hospital of Colorado Aurora, Colorado, United States
- University of South Florida Tampa, Florida, United States
Related conditions
- VLCAD deficiency (6)
- Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency (5)
- Carnitine palmitoyl transferase 2 deficiency (4)
- Carnitine-Acylcarnitine Translocase Deficiency (4)
- Medium chain acyl CoA dehydrogenase deficiency (4)
- Pathological Conditions, Signs and Symptoms (4)
- Trifunctional Protein Deficiency (4)
- Amino Acid Metabolism, Inborn Errors (3)