uric acid has been researched along with Stunted Growth in 13 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Seven male members of one family had a form of glycogen storage disease that was inherited in an X-linked recessive pattern." | 7.67 | X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardation. ( Brown, BI; DiMauro, S; Keating, JP; White, NH, 1985) |
| "Seven male members of one family had a form of glycogen storage disease that was inherited in an X-linked recessive pattern." | 3.67 | X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardation. ( Brown, BI; DiMauro, S; Keating, JP; White, NH, 1985) |
| "Primary distal renal tubular acidosis (dRTA) is an inherited disease characterized by the inability of the distal tubule to lower urine pH <5." | 1.35 | Atypical presentation of distal renal tubular acidosis in two siblings. ( Blau, N; Cheong, HI; Gucev, Z; Hoppe, B; Korneti, P; Tasic, V, 2008) |
| "Hepatomegaly was present in 39 out of 40, while 11 out of 27 reported patients had marked hepatomegaly (> 10 cm below the costal margin in the midclavicular line)." | 1.29 | The long-term outcome of patients with glycogen storage disease type Ia. ( Smit, GP, 1993) |
| "We conclude that in patients with hereditary fructose intolerance, clinically important chronic fructose intoxication can occur after infancy without causing symptoms of acute fructose intoxication and can be expressed as an apparently isolated, reversible retardation of somatic growth with a continuing disorder of adenine nucleotide metabolism, characterized in part by recurrently increased rates of degradation of adenine nucleotides." | 1.27 | Chronic fructose intoxication after infancy in children with hereditary fructose intolerance. A cause of growth retardation. ( Mock, DM; Morris, RC; Perman, JA; Thaler, M, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (61.54) | 18.7374 |
| 1990's | 1 (7.69) | 18.2507 |
| 2000's | 3 (23.08) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (7.69) | 2.80 |
| Authors | Studies |
|---|---|
| Yoon, JS | 1 |
| Seo, YJ | 1 |
| Kwon, EB | 1 |
| Lee, HJ | 1 |
| Kang, MJ | 1 |
| Hwang, IT | 1 |
| Jurecka, A | 1 |
| Tylki-Szymanska, A | 1 |
| Zikanova, M | 1 |
| Krijt, J | 1 |
| Kmoch, S | 1 |
| Sinués, B | 1 |
| Fanlo, A | 1 |
| Vicente, J | 1 |
| Mayayo-Sinués, E | 1 |
| Mayayo, E | 1 |
| Labarta, JI | 1 |
| Ferrandez-Longás, A | 1 |
| Tasic, V | 1 |
| Korneti, P | 1 |
| Gucev, Z | 1 |
| Hoppe, B | 1 |
| Blau, N | 1 |
| Cheong, HI | 1 |
| Mock, DM | 1 |
| Perman, JA | 1 |
| Thaler, M | 1 |
| Morris, RC | 1 |
| Smit, GP | 1 |
| Schaub, J | 1 |
| Spahr, RC | 1 |
| Hoyer, PF | 1 |
| Offner, G | 1 |
| Oemar, BS | 1 |
| Brodehl, J | 1 |
| Ringe, B | 1 |
| Pichlmayr, R | 1 |
| Keating, JP | 1 |
| Brown, BI | 1 |
| White, NH | 1 |
| DiMauro, S | 1 |
| Modell, CB | 1 |
| Levine, LS | 1 |
| Sonenberg, M | 1 |
| New, MI | 1 |
| Rubaltelli, FF | 1 |
| Formentin, PA | 1 |
| Tatò, L | 1 |
1 review available for uric acid and Stunted Growth
| Article | Year |
|---|---|
[The glycogenoses. Fundamentals of clinical and biochemical diagnosis].
Topics: Acidosis; Cardiomegaly; Dietary Carbohydrates; Dietary Fats; Dietary Proteins; Glycogen Storage Dise | 1978 |
12 other studies available for uric acid and Stunted Growth
| Article | Year |
|---|---|
Association between uric acid and height during growth hormone therapy in children with idiopathic short stature.
Topics: Body Height; Child; Child, Preschool; Growth Disorders; Growth Hormone; Human Growth Hormone; Humans | 2022 |
D-ribose therapy in four Polish patients with adenylosuccinate lyase deficiency: absence of positive effect.
Topics: Adenosine; Adenylosuccinate Lyase; Aminoimidazole Carboxamide; Autistic Disorder; Blood Glucose; Chi | 2008 |
Growth hormone does not alter CYP2A6 activity in growth hormone-deficient children.
Topics: Adolescent; Aryl Hydrocarbon Hydroxylases; Caffeine; Child; Child, Preschool; Chromatography, High P | 2008 |
Atypical presentation of distal renal tubular acidosis in two siblings.
Topics: Acidosis, Renal Tubular; Child, Preschool; Chlorides; Growth Disorders; Hearing Loss, Sensorineural; | 2008 |
Chronic fructose intoxication after infancy in children with hereditary fructose intolerance. A cause of growth retardation.
Topics: Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Chronic Disease; Fructose; Fructose Intole | 1983 |
The long-term outcome of patients with glycogen storage disease type Ia.
Topics: Adenoma; Adolescent; Adult; Aged; Apolipoproteins; Blood Glucose; Child; Cholesterol; Female; Glycog | 1993 |
Von Gierke's disease: a review.
Topics: Allopurinol; Bicarbonates; Blood Glucose; Diazoxide; Gluconeogenesis; Glucose-6-Phosphatase; Glycoge | 1976 |
Four years' experience with cyclosporine A in pediatric kidney transplantation.
Topics: Child; Cyclosporins; Dose-Response Relationship, Drug; Glomerular Filtration Rate; Graft Survival; G | 1988 |
X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardation.
Topics: Adolescent; Adult; Biopsy; Child; Glycogen; Glycogen Debranching Enzyme System; Glycogen Storage Dis | 1985 |
Haemoglobinopathies. The pathophysiology of beta-thalassaemia major.
Topics: Adolescent; Child; Child, Preschool; Creatinine; Erythropoiesis; Growth Disorders; Hemoglobins; Homo | 1974 |
Metabolic effects in children of a 37 amino acid fragment of bovine growth hormone.
Topics: Adenoma, Chromophobe; Adolescent; Alkaline Phosphatase; Amino Acids; Blood Urea Nitrogen; Calcium; C | 1973 |
Ammonia nitrogen, urea and uric acid blood levels in normal and hypodystrophic newborns.
Topics: Ammonia; Blood Urea Nitrogen; Embryonic and Fetal Development; Fetus; Growth Disorders; Humans; Infa | 1970 |