uric acid has been researched along with Galactosemias in 7 studies
Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.
Galactosemias: A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)
| Excerpt | Relevance | Reference |
|---|---|---|
| "In two patients with hereditary fructose intolerance (HFI) the peak blood uric acid levels were 12." | 1.25 | Fructose-induced hyperuricemia: observations in normal children and in patients with hereditary fructose intolerance and galactosemia. ( Kogut, MD; Ng, W; Nonnel, GN; Roe, TF, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (85.71) | 18.7374 |
| 1990's | 1 (14.29) | 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 |
|---|---|
| Heuckenkamp, PU | 1 |
| Zöllner, N | 1 |
| Kogut, MD | 1 |
| Roe, TF | 1 |
| Ng, W | 1 |
| Nonnel, GN | 1 |
| Forster, J | 1 |
| Schuchmann, L | 1 |
| Hans, C | 1 |
| Niederhoff, H | 1 |
| Künzer, W | 1 |
| Keppler, D | 1 |
| Szczypka, M | 1 |
| Gajewski, J | 1 |
| Laskowska-Klita, T | 1 |
| Zbieg-Sendecka, E | 1 |
| Pronicka, E | 1 |
| Rowińska, E | 1 |
| Miłoszewska, E | 1 |
| Holtzman, NA | 1 |
| Förster, H | 1 |
| Haslbeck, M | 1 |
1 review available for uric acid and Galactosemias
| Article | Year |
|---|---|
Dietary treatment of inborn errors of metabolism.
Topics: Ammonia; Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Female; Fructose; Galactosemias; Glyc | 1970 |
6 other studies available for uric acid and Galactosemias
| Article | Year |
|---|---|
Quantitative comparison and evaluation of utilization of parenteral administered carbohydrates.
Topics: Blood Glucose; Dietary Carbohydrates; Ethanol; Fructose; Galactose; Galactosemias; Glucose; Glycosur | 1975 |
Fructose-induced hyperuricemia: observations in normal children and in patients with hereditary fructose intolerance and galactosemia.
Topics: Adult; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Fruct | 1975 |
Increased serum urate in galactosemia patients after a galactose load: a possible role of nucleotide deficiency in galactosemic liver injury.
Topics: Blood Glucose; Child; Erythrocytes; Galactose; Galactosemias; Humans; Liver Diseases; UDPglucose-Hex | 1975 |
Red blood cells and serum antioxidant defense systems of galactosaemic children.
Topics: Antioxidants; Cataract; Ceruloplasmin; Child; Child, Preschool; Erythrocytes; Galactosemias; Humans; | 1990 |
Tubular function of kidney after galactose loading in two patients with glycogen storage disease type XL.
Topics: Adolescent; Adult; Bicarbonates; Fanconi Syndrome; Galactose; Galactosemias; Glycogen Storage Diseas | 1987 |
[Studies on the enzymatic determination of galactose with galactose oxidase].
Topics: Acetates; Alcohol Oxidoreductases; Aniline Compounds; Barbiturates; Blood Chemical Analysis; Buffers | 1967 |