uric acid has been researched along with Cerebral Palsy in 19 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.
Cerebral Palsy: A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
| Excerpt | Relevance | Reference |
|---|---|---|
| " Hyperuricemia leads to hyperuricuria and uric acid nephrolithiasis." | 3.74 | Rare variant of Lesch-Nyhan syndrome without self-mutilation or nephrolithiasis. ( Kersnik Levart, T, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (68.42) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (10.53) | 29.6817 |
| 2010's | 3 (15.79) | 24.3611 |
| 2020's | 1 (5.26) | 2.80 |
| Authors | Studies |
|---|---|
| Ambarsari, CG | 1 |
| Cahyadi, D | 1 |
| Sari, L | 1 |
| Satria, O | 1 |
| Sahli, F | 1 |
| Darmadi, TL | 1 |
| Kadaristiana, A | 1 |
| Ayyavoo, A | 1 |
| Derraik, JG | 1 |
| Hofman, PL | 1 |
| Cutfield, WS | 1 |
| Schoendorfer, N | 1 |
| Tinggi, U | 1 |
| Sharp, N | 2 |
| Boyd, R | 1 |
| Vitetta, L | 2 |
| Davies, PS | 2 |
| Schoendorfer, NC | 1 |
| Obeid, R | 1 |
| Moxon-Lester, L | 1 |
| Boyd, RN | 1 |
| LESCH, M | 2 |
| NYHAN, WL | 2 |
| HOEFNAGEL, D | 1 |
| Aycicek, A | 1 |
| Iscan, A | 1 |
| Kersnik Levart, T | 1 |
| van der Zee, SP | 1 |
| Schretlen, ED | 1 |
| Monnens, LA | 1 |
| Kekre, S | 1 |
| Singh, SD | 1 |
| Chhaparwal, BC | 1 |
| Pohowalla, JN | 1 |
| Sweetman, L | 1 |
| Seegmiller, JE | 2 |
| Kastner, C | 1 |
| Manzke, H | 1 |
| Becker, MH | 1 |
| Wallin, JK | 1 |
| Kaufman, JM | 1 |
| Greene, ML | 1 |
| Byrne, WL | 1 |
| Sass, JK | 1 |
| Itabashi, HH | 1 |
| Dexter, RA | 1 |
| Dodge, PR | 1 |
2 reviews available for uric acid and Cerebral Palsy
| Article | Year |
|---|---|
Uric acid studies in serum and cerebrospinal fluid in neurological disorders with mental retardation.
Topics: Carbohydrate Metabolism, Inborn Errors; Central Nervous System Diseases; Cerebral Palsy; Child; Chil | 1971 |
Biochemical and genetic studies of an X-linked neurological disease (The Lesch-Nyhan syndrome).
Topics: Animals; Athetosis; Cells, Cultured; Cerebral Palsy; Child; Disease Models, Animal; Feedback; Female | 1971 |
1 trial available for uric acid and Cerebral Palsy
| Article | Year |
|---|---|
Effects of the uricogenic agent, 2-ethylamino-1,3,4-thiadiazole in hypoxanthine-guanine phosphoribosyl transferase deficiency.
Topics: Adolescent; Athetosis; Azoles; Carbon Isotopes; Cerebral Palsy; Child; Chorea; Clinical Trials as To | 1968 |
16 other studies available for uric acid and Cerebral Palsy
| Article | Year |
|---|---|
Late diagnosis of Lesch-Nyhan disease complicated with end-stage renal disease and tophi burst: a case report.
Topics: Adolescent; Allopurinol; Cerebral Palsy; Delayed Diagnosis; Exons; Gout Suppressants; Humans; Hypoxa | 2020 |
Postterm births: are prolonged pregnancies too long?
Topics: Body Composition; Body Mass Index; Cerebral Palsy; Child Behavior Disorders; Child, Preschool; Diabe | 2014 |
Protein levels in enteral feeds: do these meet requirements in children with severe cerebral palsy?
Topics: Albumins; Blood Proteins; Case-Control Studies; Cerebral Palsy; Child; Child, Preschool; Creatinine; | 2012 |
Methylation capacity in children with severe cerebral palsy.
Topics: Betaine; Biomarkers; Case-Control Studies; Cerebral Palsy; Child; Child, Preschool; Choline; Cystath | 2012 |
A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION.
Topics: Athetosis; Biomedical Research; Blood Chemical Analysis; Central Nervous System Diseases; Cerebral P | 1964 |
THE SYNDROME OF ATHETOID CEREBRAL PALSY, MENTAL DEFICIENCY, SELF-MUTILATION AND HYPERURICEMIA.
Topics: Athetosis; Blood Chemical Analysis; Blood Urea Nitrogen; Cerebral Palsy; Child; Genetics, Medical; H | 1965 |
Oxidative and antioxidative capacity in children with cerebral palsy.
Topics: Albumins; Analysis of Variance; Cerebral Palsy; Child; Child, Preschool; Female; Humans; Infant; Lip | 2006 |
Rare variant of Lesch-Nyhan syndrome without self-mutilation or nephrolithiasis.
Topics: Cerebral Palsy; Child; Diagnosis, Differential; Humans; Kidney; Lesch-Nyhan Syndrome; Male; Nephroca | 2007 |
Megaloblastic anaemia in the Lesch-Nyhan syndrome.
Topics: Adenine; Anemia, Macrocytic; Cerebral Palsy; Child; Humans; Intellectual Disability; Male; Movement | 1968 |
[Juvenile hyperuricemia, gout and cerebral palsy (Lesch-Nyhan syndrome)].
Topics: Adolescent; Allopurinol; Athetosis; Cerebral Palsy; Chorea; Gout; Humans; Male; Uric Acid | 1969 |
[Hyperuricemia with cerebral paresis. Syndrome of a hereditary purine metabolic disorder].
Topics: Adolescent; Anemia, Macrocytic; Cerebral Palsy; Child; Child, Preschool; Glycine; Humans; Hyperlipid | 1967 |
Congenital hyperuricosuria. Associated radiologic features.
Topics: Cerebral Palsy; Child; Finger Injuries; Gout; Hip Dislocation; Humans; Intellectual Disability; Male | 1968 |
Urine uric acid to creatinine rtio--a screening test for inherited disorders of purine metabolism. Phosphoribosyltransferase (PRT) deficiency in X-linked cerebral palsy and in a variant of gout.
Topics: Adolescent; Adult; Age Factors; Aged; Cerebral Palsy; Child; Child, Preschool; Creatinine; Diet; Fem | 1968 |
Molecular approaches to the central nervous system: AAAS Symposium 29-31 December 1968. Dallas, Texas.
Topics: Athetosis; Cerebral Palsy; Chorea; Glucosyltransferases; Humans; Intellectual Disability; Molecular | 1968 |
Juvenile gout with brain involvement.
Topics: Blood; Brain; Cerebral Palsy; Child; Demyelinating Diseases; Gout; Humans; Intellectual Disability; | 1965 |
Disordered uric acid metabolism and neurologic abnormalities.
Topics: Blood-Brain Barrier; Cerebral Palsy; Humans; Infant; Intellectual Disability; Male; Movement Disorde | 1966 |