corticosterone has been researched along with Smith-Lemli-Opitz Syndrome in 1 studies
Smith-Lemli-Opitz Syndrome: An autosomal recessive disorder of CHOLESTEROL metabolism. It is caused by a deficiency of 7-dehydrocholesterol reductase, the enzyme that converts 7-dehydrocholesterol to cholesterol, leading to an abnormally low plasma cholesterol. This syndrome is characterized by multiple CONGENITAL ABNORMALITIES, growth deficiency, and INTELLECTUAL DISABILITY.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Matabosch, X | 1 |
Rahman, M | 1 |
Hughes, B | 1 |
Patel, SB | 1 |
Watson, G | 1 |
Shackleton, C | 1 |
1 other study available for corticosterone and Smith-Lemli-Opitz Syndrome
Article | Year |
---|---|
Steroid production and excretion by the pregnant mouse, particularly in relation to pregnancies with fetuses deficient in Delta7-sterol reductase (Dhcr7), the enzyme associated with Smith-Lemli-Opitz syndrome.
Topics: Animals; Animals, Newborn; Cholesterol; Corticosterone; Female; Fetus; Gas Chromatography-Mass Spect | 2009 |