Page last updated: 2024-10-15

acetylcarnitine and Biotinidase Deficiency

acetylcarnitine has been researched along with Biotinidase Deficiency in 1 studies

Acetylcarnitine: An acetic acid ester of CARNITINE that facilitates movement of ACETYL COA into the matrices of mammalian MITOCHONDRIA during the oxidation of FATTY ACIDS.

Biotinidase Deficiency: The late onset form of MULTIPLE CARBOXYLASE DEFICIENCY (deficiency of the activities of biotin-dependent enzymes propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to a defect or deficiency in biotinidase which is essential for recycling BIOTIN.

Research Excerpts

ExcerptRelevanceReference
"We found biotinidase deficiency in NS with a mean 1."1.48Could nodding syndrome in Northern Uganda be a form of autism spectrum disorder? an observational study design. ( Arony, DA; Gazda, S; Kitara, DL, 2018)

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
Arony, DA1
Gazda, S1
Kitara, DL1

Other Studies

1 other study available for acetylcarnitine and Biotinidase Deficiency

ArticleYear
Could nodding syndrome in Northern Uganda be a form of autism spectrum disorder? an observational study design.
    The Pan African medical journal, 2018, Volume: 30

    Topics: Acetylcarnitine; Adolescent; Autism Spectrum Disorder; Biotinidase Deficiency; Child; Environmental

2018