uric acid has been researched along with Pseudohypoparathyroidism in 3 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.
Pseudohypoparathyroidism: A hereditary syndrome clinically similar to HYPOPARATHYROIDISM. It is characterized by HYPOCALCEMIA; HYPERPHOSPHATEMIA; and associated skeletal development impairment and caused by failure of response to PARATHYROID HORMONE rather than deficiencies. A severe form with resistance to multiple hormones is referred to as Type 1a and is associated with maternal mutant allele of the ALPHA CHAIN OF STIMULATORY G PROTEIN.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Furthermore, the findings in the index case present interesting novel aspects, including a previously undescribed coexistence of the 3-kb STX16 deletion and AHO-like features and a clinical course complicated by concomitant 25-[OH]-vitamin D deficiency, which may have resulted, at least partly, from long-term use of antiepileptic drugs." | 5.35 | Molecular diagnosis and clinical characterization of pseudohypoparathyroidism type-Ib in a patient with mild Albright's hereditary osteodystrophy-like features, epileptic seizures, and defective renal handling of uric acid. ( Babaoglu, M; Bastepe, M; Bayraktar, M; Harmanci, A; Unluturk, U; Varli, K; Yasar, U, 2008) |
| " Furthermore, the findings in the index case present interesting novel aspects, including a previously undescribed coexistence of the 3-kb STX16 deletion and AHO-like features and a clinical course complicated by concomitant 25-[OH]-vitamin D deficiency, which may have resulted, at least partly, from long-term use of antiepileptic drugs." | 1.35 | Molecular diagnosis and clinical characterization of pseudohypoparathyroidism type-Ib in a patient with mild Albright's hereditary osteodystrophy-like features, epileptic seizures, and defective renal handling of uric acid. ( Babaoglu, M; Bastepe, M; Bayraktar, M; Harmanci, A; Unluturk, U; Varli, K; Yasar, U, 2008) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Unluturk, U | 1 |
| Harmanci, A | 1 |
| Babaoglu, M | 1 |
| Yasar, U | 1 |
| Varli, K | 1 |
| Bastepe, M | 2 |
| Bayraktar, M | 1 |
| Laspa, E | 1 |
| Jüppner, H | 1 |
| Tsatsoulis, A | 1 |
| Hafezi, FF | 1 |
3 other studies available for uric acid and Pseudohypoparathyroidism
| Article | Year |
|---|---|
Molecular diagnosis and clinical characterization of pseudohypoparathyroidism type-Ib in a patient with mild Albright's hereditary osteodystrophy-like features, epileptic seizures, and defective renal handling of uric acid.
Topics: Adolescent; Anticonvulsants; Base Sequence; Brain; Chronic Kidney Disease-Mineral and Bone Disorder; | 2008 |
Phenotypic and molecular genetic aspects of pseudohypoparathyroidism type Ib in a Greek kindred: evidence for enhanced uric acid excretion due to parathyroid hormone resistance.
Topics: Adult; Chromogranins; Chromosomes, Human, Pair 20; Drug Resistance; Genetic Linkage; Greece; GTP-Bin | 2004 |
Recurrent congenital coxa vara associated with primary hypoparathyroidism. A case report.
Topics: Alkaline Phosphatase; Calcium; Child; Creatinine; Diagnosis, Differential; Female; Hip; Humans; Hype | 1971 |