meglutol has been researched along with Diseases in Twins in 3 studies
Meglutol: An antilipemic agent which lowers cholesterol, triglycerides, serum beta-lipoproteins and phospholipids. It acts by interfering with the enzymatic steps involved in the conversion of acetate to hydroxymethylglutaryl coenzyme A as well as inhibiting the activity of HYDROXYMETHYLGLUTARYL COA REDUCTASES which is the rate limiting enzyme in the biosynthesis of cholesterol.
3-hydroxy-3-methylglutaric acid : A dicarboxylic acid that is glutaric acid in which one of the two hydrogens at position 3 is substituted by a hydroxy group, while the other is substituted by a methyl group. It has been found to accumulate in urine of patients suffering from HMG-CoA lyase (3-hydroxy-3-methylglutaryl-CoA lyase, EC 4.1.3.4) deficiency. It occurs as a plant metabolite in Crotalaria dura.
Diseases in Twins: Disorders affecting TWINS, one or both, at any age.
| Excerpt | Relevance | Reference |
|---|---|---|
| "A 4-month-old infant with hypotonia and macrocephaly was diagnosed as having 3-hydroxy-3-methylglutaric aciduria, using gas chromatography and mass spectrometry and confirmatory enzyme studies." | 1.27 | Dizygotic twins with 3-hydroxy-3-methylglutaric aciduria; unusual presentation, family studies and dietary management. ( Chalmers, RA; de Sousa, C; Mistry, J; Stacey, TE; Timbrell, P; Tracey, BM; Whitelaw, A, 1985) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gibson, KM | 1 |
| Lee, CF | 1 |
| Wappner, RS | 1 |
| Thompson, GN | 1 |
| Chalmers, RA | 2 |
| Halliday, D | 1 |
| Stacey, TE | 1 |
| de Sousa, C | 1 |
| Tracey, BM | 1 |
| Whitelaw, A | 1 |
| Mistry, J | 1 |
| Timbrell, P | 1 |
3 other studies available for meglutol and Diseases in Twins
| Article | Year |
|---|---|
3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case.
Topics: Carnitine; Diseases in Twins; Fibroblasts; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Lympho | 1992 |
The contribution of protein catabolism to metabolic decompensation in 3-hydroxy-3-methylglutaric aciduria.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Diseases in Twins; Female; Glutarates; Humans; Leucine; | 1990 |
Dizygotic twins with 3-hydroxy-3-methylglutaric aciduria; unusual presentation, family studies and dietary management.
Topics: Acidosis; Brain; Chromatography, Gas; Diet; Diseases in Twins; Female; Glutarates; Humans; Infant; M | 1985 |