glycine has been researched along with Adrenal Hyperplasia, Congenital in 4 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hershkovitz, E | 1 |
| Parvari, R | 1 |
| Wudy, SA | 1 |
| Hartmann, MF | 1 |
| Gomes, LG | 1 |
| Loewental, N | 1 |
| Miller, WL | 1 |
| Yang, LX | 1 |
| Toda, K | 1 |
| Miyahara, K | 1 |
| Nomoto, S | 1 |
| Kinoshita, E | 1 |
| Baba, T | 1 |
| Yoshimoto, M | 1 |
| Araki, K | 1 |
| Kurashige, T | 1 |
| Hashimoto, K | 1 |
| Nakagawa, Y | 1 |
| Yamada, M | 1 |
| Ogawa, H | 1 |
| Igarashi, Y | 1 |
| Omenn, GS | 1 |
1 review available for glycine and Adrenal Hyperplasia, Congenital
| Article | Year |
|---|---|
Inborn errors of metabolism: clues to understanding human behavioral disorders.
Topics: Adrenal Hyperplasia, Congenital; Brain; Galactosemias; Glycine; Hepatolenticular Degeneration; Heter | 1976 |
3 other studies available for glycine and Adrenal Hyperplasia, Congenital
| Article | Year |
|---|---|
Homozygous mutation G539R in the gene for P450 oxidoreductase in a family previously diagnosed as having 17,20-lyase deficiency.
Topics: Adrenal Hyperplasia, Congenital; Adult; Arginine; Base Sequence; Consanguinity; Diagnosis, Different | 2008 |
Classic steroid 11 beta-hydroxylase deficiency caused by a C-->G transversion in exon 7 of CYP11B1.
Topics: Adolescent; Adrenal Hyperplasia, Congenital; Amino Acid Sequence; Arginine; Base Sequence; Consangui | 1995 |
Missense mutation in CYP11B1 (CGA[Arg-384]-->GGA[Gly]) causes steroid 11 beta-hydroxylase deficiency.
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Sequence; Arginine; Base Sequence; Child; Cytochrome P-4 | 1995 |