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uric acid and Congenital Hypothyroidism

uric acid has been researched along with Congenital Hypothyroidism in 2 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.

Congenital Hypothyroidism: A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19902 (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
Khalil, M1
el-Khateeb, S1
Aref, GH1
Guirgis, FK1
Kekre, S1
Singh, SD1
Chhaparwal, BC1
Pohowalla, JN1

Reviews

1 review available for uric acid and Congenital Hypothyroidism

ArticleYear
Uric acid studies in serum and cerebrospinal fluid in neurological disorders with mental retardation.
    Indian pediatrics, 1971, Volume: 8, Issue:10

    Topics: Carbohydrate Metabolism, Inborn Errors; Central Nervous System Diseases; Cerebral Palsy; Child; Chil

1971

Other Studies

1 other study available for uric acid and Congenital Hypothyroidism

ArticleYear
Plasma uric acid in infants and children.
    The Journal of tropical medicine and hygiene, 1967, Volume: 70, Issue:1

    Topics: Adult; Congenital Hypothyroidism; Down Syndrome; Female; Humans; In Vitro Techniques; Infant; Infant

1967