androsterone 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 |
---|---|
Marcos, J | 1 |
Craig, WY | 1 |
Palomaki, GE | 1 |
Kloza, EM | 1 |
Haddow, JE | 1 |
Roberson, M | 1 |
Bradley, LA | 1 |
Shackleton, CH | 1 |
1 other study available for androsterone and Smith-Lemli-Opitz Syndrome
Article | Year |
---|---|
Maternal urine and serum steroid measurements to identify steroid sulfatase deficiency (STSD) in second trimester pregnancies.
Topics: Androsterone; Dehydroepiandrosterone; Estriol; False Positive Reactions; Female; Gas Chromatography- | 2009 |