acetone has been researched along with Glycogen Storage Disease Type I in 1 studies
methyl ketone : A ketone of formula RC(=O)CH3 (R =/= H).
Glycogen Storage Disease Type I: An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Fernandes, J | 1 |
| Pikaar, NA | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Anaplerotic Therapy Using Triheptanoin for Patients With Glycogen Storage Disease Type I[NCT03665636] | Early Phase 1 | 4 participants (Actual) | Interventional | 2020-10-16 | Completed | ||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
1 other study available for acetone and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Ketosis in hepatic glycogenosis.
Topics: Acetone; Acidosis; Adolescent; Adult; Age Factors; Blood Glucose; Caseins; Child; Child, Preschool; | 1972 |