urea has been researched along with Netherton Syndrome in 1 studies
pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
Netherton Syndrome: Rare autosomal recessive disease with variable expressions. Clinical features of the disease include variable ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; bamboo hair (trichorrhexis invaginata); and ATOPIC DERMATITIS. The disease is caused by mutations in the SPINK5 gene.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kogut, M | 1 |
| Salz, M | 1 |
| Hadaschik, EN | 1 |
| Kohlhase, J | 1 |
| Hartmann, M | 1 |
1 other study available for urea and Netherton Syndrome
| Article | Year |
|---|---|
New mutation leading to the full variety of typical features of the Netherton syndrome.
Topics: Calcineurin Inhibitors; Dermatologic Agents; Diagnosis, Differential; Female; Genetic Markers; Genet | 2015 |