1 completed. .
Follow 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency: new trials by email Literature Review of 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency trials Research Report on 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| Baby Detect : Genomic Newborn Screening Congenital Adrenal Hyperplasia, Familial Hyperinsulinemic Hypoglycemia 1 | Completed | Centre Hospitalier Universitaire de Liege | 6824 | 2022-09-01 | 2025-08-12 |
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (1) · Acidemia, isovaleric (1) · Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of (1) · Adrenal Hyperplasia, Congenital (1) · Adrenoleukodystrophy (1) · Andersen Syndrome (1) · Anemia, Diamond-Blackfan (1) · Anemia, Sickle Cell (1) · Argininosuccinic Aciduria (1) · Aromatic amino acid decarboxylase deficiency (1) · Aspartylglucosaminuria (1) · Ataxia with vitamin E deficiency (1) · Basal ganglia disease, biotin-responsive (1) · Beta ketothiolase deficiency (1)
Abnormalities, Multiple (1) · Adrenal Gland Diseases (1) · Adrenal Insufficiency (1) · Adrenogenital Syndrome (1) · Albinism (1) · Amino Acid Metabolism, Inborn Errors (1) · Anemia (1) · Anemia, Aplastic (1) · Anemia, Hemolytic (1) · Anemia, Hemolytic, Congenital (1) · Anemia, Hypoplastic, Congenital (1) · Arrhythmias, Cardiac (1) · Autoimmune Diseases (1) · Autoimmune Diseases of the Nervous System (1) · Avitaminosis (1)
Centre Hospitalier Universitaire de Liege (1)
Belgium (1)
Laurent Servais (1)