prednisolone has been researched along with Mevalonate Kinase Deficiency in 1 studies
Prednisolone: A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states.
prednisolone : A glucocorticoid that is prednisone in which the oxo group at position 11 has been reduced to the corresponding beta-hydroxy group. It is a drug metabolite of prednisone.
Mevalonate Kinase Deficiency: Autosomal recessive disorder caused by mutations in the mevalonate kinase gene. Because of the mutations cholesterol biosynthesis is disrupted and MEVALONIC ACID accumulates. It is characterized by a range of symptoms, including dysmorphic FACIES, psychomotor retardation, CATARACT, hepatosplenomegaly, CEREBELLAR ATAXIA, elevated IMMUNOGLOBULIN D, and recurrent febrile crises with FEVER; LYMPHADENOPATHY; ARTHRALGIA; EDEMA; and rash.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Prednisolone was administered on each attack, and her febrile attack has been controlled well since she was diagnosed with MKD." | 1.46 | A 6-year-old girl diagnosed with mevalonate kinase deficiency who had hydrops fetalis and neonatal-onset cholestasis. ( Heike, T; Hiramoto, R; Inui, A; Komori, I; Matsumoto, S; Nishikomori, R; Tanaka, T; Umetsu, S; Yamashita, Y, 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 |
|---|---|
| Yamashita, Y | 1 |
| Matsumoto, S | 1 |
| Hiramoto, R | 1 |
| Komori, I | 1 |
| Tanaka, T | 1 |
| Nishikomori, R | 1 |
| Heike, T | 1 |
| Umetsu, S | 1 |
| Inui, A | 1 |
1 other study available for prednisolone and Mevalonate Kinase Deficiency
| Article | Year |
|---|---|
A 6-year-old girl diagnosed with mevalonate kinase deficiency who had hydrops fetalis and neonatal-onset cholestasis.
Topics: Anemia; Biomarkers; Child; Cholestasis; Edema; Female; Genetic Testing; Humans; Immunoglobulin D; Me | 2017 |