fr 74366 has been researched along with Galactosemias in 1 studies
Galactosemias: A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ikebe, H | 1 |
| Terubayashi, H | 1 |
| Okamoto, S | 1 |
| Matsumoto, Y | 1 |
| Tsutsumi, M | 1 |
| Ibaraki, N | 1 |
| Akagi, Y | 1 |
1 other study available for fr 74366 and Galactosemias
| Article | Year |
|---|---|
[Ciliary body changes associate with aldose reductase in galactosemic rats (2)].
Topics: Aldehyde Reductase; Animals; Ciliary Body; Epithelium; Galactosemias; Hypertrophy; Quinazolines; Rat | 1992 |