pramoxine has been researched along with Alagille Syndrome in 1 studies
pramoxine: RN given refers to parent cpd; structure
pramocaine : A member of the class of morpholines that is morpholine substituted at the nitrogen atom by a 3-(4-butoxyphenoxy)propyl group.
Alagille Syndrome: A multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC), and malformations in the cardiovascular system, the eyes, the vertebral column, and the facies. Major clinical features include JAUNDICE, and congenital heart disease with peripheral PULMONARY STENOSIS. Alagille syndrome may result from heterogeneous gene mutations, including mutations in JAG1 on CHROMOSOME 20 (Type 1) and NOTCH2 on CHROMOSOME 1 (Type 2).
| Excerpt | Relevance | Reference |
|---|---|---|
| "When encountered in children, xanthomas are most commonly associated with a group of disorders known as familial hyperlipidemias." | 2.55 | The triad of pruritus, xanthomas, and cholestasis: Two cases and a brief review of the literature. ( Jacks, SK; Mosser, JL; Pearson, HJ, 2017) |
| 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 |
|---|---|
| Pearson, HJ | 1 |
| Mosser, JL | 1 |
| Jacks, SK | 1 |
1 review available for pramoxine and Alagille Syndrome
| Article | Year |
|---|---|
The triad of pruritus, xanthomas, and cholestasis: Two cases and a brief review of the literature.
Topics: Abnormalities, Multiple; Alagille Syndrome; Anesthetics, Local; Ataxia; Brain; Child; Child, Prescho | 2017 |