Page last updated: 2024-10-19

orotic acid and Coma

orotic acid has been researched along with Coma in 7 studies

Orotic Acid: An intermediate product in PYRIMIDINE synthesis which plays a role in chemical conversions between DIHYDROFOLATE and TETRAHYDROFOLATE.
orotic acid : A pyrimidinemonocarboxylic acid that is uracil bearing a carboxy substituent at position C-6.

Coma: A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs when there is dysfunction or injury involving both cerebral hemispheres or the brain stem RETICULAR FORMATION.

Research Excerpts

ExcerptRelevanceReference
" Crystalluria in a three-month-old male infant with a history of intermittent vomiting since birth and incipient coma led to the discovery of orotic aciduria."3.65Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant. ( Mackenzie, S; MacLeod, P; Scriver, CR, 1972)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19907 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Coskun, T1
Ozalp, I1
Mönch, S1
Kneer, J1
Girgis, N1
McGravey, V1
Shah, BL1
Herrin, J1
Shih, VE1
Rottem, M1
Statter, M1
Amit, R1
Brand, N1
Bujanover, Y1
Yatziv, S1
Rowe, PC1
Newman, SL1
Brusilow, SW1
Batshaw, ML1
Sunshine, P1
Lindenbaum, JE1
Levy, HL1
Freeman, JM1
MacLeod, P1
Mackenzie, S1
Scriver, CR1

Other Studies

7 other studies available for orotic acid and Coma

ArticleYear
Lethal hyperammonaemic coma due to ornithine transcarbamylase deficiency presenting as brain stem encephalitis in a previously asymptomatic ten-year-old boy.
    Journal of inherited metabolic disease, 1987, Volume: 10, Issue:3

    Topics: Ammonia; Brain Stem; Child; Citrulline; Coma; Diagnosis, Differential; Encephalitis; Humans; Male; O

1987
Lethal ornithine transcarbamylase deficiency in a female neonate.
    Journal of inherited metabolic disease, 1987, Volume: 10, Issue:3

    Topics: Ammonia; Arginine; Citrulline; Coma; Female; Humans; Infant, Newborn; Ornithine Carbamoyltransferase

1987
Clinical and laboratory study in 22 patients with inherited hyperammonemic syndromes.
    Israel journal of medical sciences, 1986, Volume: 22, Issue:11

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Coma; Female; Humans; Male; Orotic Acid; Pedig

1986
Natural history of symptomatic partial ornithine transcarbamylase deficiency.
    The New England journal of medicine, 1986, Feb-27, Volume: 314, Issue:9

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Ataxia; Child, Preschool; Coma; Diagnosis, Differenti

1986
The diagnosis of ornithine transcarbamylase deficiency.
    Journal of pediatric gastroenterology and nutrition, 1985, Volume: 4, Issue:1

    Topics: Animals; Carbamyl Phosphate; Citrulline; Coma; Female; Humans; Infant; Infant, Newborn; Intellectual

1985
Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.
    Pediatrics, 1972, Volume: 50, Issue:1

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Central Nervous System Diseases; Child; Child

1972
Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant.
    Canadian Medical Association journal, 1972, Sep-09, Volume: 107, Issue:5

    Topics: Ammonia; Chromatography, Gas; Coma; Humans; Infant; Infusions, Parenteral; Liver; Male; Metabolism,

1972
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