Page last updated: 2024-10-16

acetone and Genetic Diseases, Inborn

acetone has been researched along with Genetic Diseases, Inborn in 1 studies

methyl ketone : A ketone of formula RC(=O)CH3 (R =/= H).

Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Shroads, AL1
Coats, BS1
McDonough, CW1
Langaee, T1
Stacpoole, PW1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Phase 3 Trial of Dichloroacetate in Pyruvate Dehydrogenase Complex Deficiency:[NCT02616484]Phase 334 participants (Actual)Interventional2020-07-14Active, not recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trials

1 trial available for acetone and Genetic Diseases, Inborn

ArticleYear
Haplotype variations in glutathione transferase zeta 1 influence the kinetics and dynamics of chronic dichloroacetate in children.
    Journal of clinical pharmacology, 2015, Volume: 55, Issue:1

    Topics: Acetone; Adolescent; Adult; Aminolevulinic Acid; Child; Child, Preschool; Dichloroacetic Acid; Doubl

2015