Page last updated: 2024-10-20

thymine and Adrenal Hyperplasia, Congenital

thymine has been researched along with Adrenal Hyperplasia, Congenital in 1 studies

Adrenal Hyperplasia, Congenital: A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Nguyen, TP1
Nguyen, TH1
Ngo, DN1
Vu, CD1
Nguyen, TK1
Nong, VH1
Nguyen, HH1

Other Studies

1 other study available for thymine and Adrenal Hyperplasia, Congenital

ArticleYear
A novel homozygous mutation IVS6+5G>T in CYP11B1 gene in a Vietnamese patient with 11β-hydroxylase deficiency.
    Gene, 2015, Jul-10, Volume: 565, Issue:2

    Topics: Adrenal Hyperplasia, Congenital; Asian People; Guanine; Homozygote; Humans; Introns; Male; Mutation;

2015