Page last updated: 2024-10-16

carnitine and Developmental Disabilities

carnitine has been researched along with Developmental Disabilities in 6 studies

Developmental Disabilities: Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed)

Research Excerpts

ExcerptRelevanceReference
"An infant with delayed development and peripheral myopathy, nourished on a soy-based liquid diet deficient in carnitine, had gastrointestinal dysmotility manifested by postprandial vomiting, oral drooling, delayed gastric emptying and infrequent bowel movements."3.68Carnitine deficiency: a possible cause of gastrointestinal dysmotility. ( Gladstone, W; Rosenthal, SR; Weaver, LT; Winter, HS, 1992)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (33.33)18.2507
2000's1 (16.67)29.6817
2010's2 (33.33)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Kirby, T1
Walters, DC1
Brown, M1
Jansen, E1
Salomons, GS1
Turgeon, C1
Rinaldo, P1
Arning, E1
Ashcraft, P1
Bottiglieri, T1
Roullet, JB1
Gibson, KM1
Waisbren, SE1
Landau, Y1
Wilson, J1
Vockley, J1
Pollard, LM1
Williams, NR1
Espinoza, L1
Wood, TC1
Spector, EB1
Schroer, RJ1
Holden, KR1
Gordon, N1
Bratton, SL1
Garden, AL1
Bohan, TP1
French, JW1
Clarke, WR1
Weaver, LT1
Rosenthal, SR1
Gladstone, W1
Winter, HS1

Other Studies

6 other studies available for carnitine and Developmental Disabilities

ArticleYear
Post-mortem tissue analyses in a patient with succinic semialdehyde dehydrogenase deficiency (SSADHD). I. Metabolomic outcomes.
    Metabolic brain disease, 2020, Volume: 35, Issue:4

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Brain; Carnitine; Creatine; Creatinine; De

2020
Neuropsychological outcomes in fatty acid oxidation disorders: 85 cases detected by newborn screening.
    Developmental disabilities research reviews, 2013, Volume: 17, Issue:3

    Topics: Acyl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Developmental Disabilities; Fatty Acids;

2013
Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency.
    Journal of child neurology, 2010, Volume: 25, Issue:8

    Topics: Brain Diseases, Metabolic; Carnitine; Child; Child, Preschool; Developmental Disabilities; Female; H

2010
Acyl-CoA dehydrogenase deficiency: varieties with neurological involvement.
    Developmental medicine and child neurology, 2005, Volume: 47, Issue:3

    Topics: Acyl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Chromosome Aberrations; Developmental Di

2005
A child with valproic acid-associated carnitine deficiency and carnitine-responsive cardiac dysfunction.
    Journal of child neurology, 1992, Volume: 7, Issue:4

    Topics: Carnitine; Child; Developmental Disabilities; Heart Diseases; Humans; Male; Metabolic Diseases; Myoc

1992
Carnitine deficiency: a possible cause of gastrointestinal dysmotility.
    Acta paediatrica (Oslo, Norway : 1992), 1992, Volume: 81, Issue:1

    Topics: Bottle Feeding; Carnitine; Child, Preschool; Constipation; Developmental Disabilities; Food, Fortifi

1992