hydroxyurea has been researched along with Porphyria Cutanea Tarda in 1 studies
Porphyria Cutanea Tarda: An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form.
| Excerpt | Relevance | Reference |
|---|---|---|
| "A 70-year-old man with primary myelofibrosis was treated with hydroxycarbamide and blood transfusions." | 1.31 | [Diagnostic image (117). A man with frequent blood transfusion and blister on his fingers. A form of porpheria cutanea tarda caused by excess iron]. ( Jonkhoff, AR; van der Valk, P; Zweegman, S, 2002) |
| 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 |
|---|---|
| Zweegman, S | 1 |
| van der Valk, P | 1 |
| Jonkhoff, AR | 1 |
1 other study available for hydroxyurea and Porphyria Cutanea Tarda
| Article | Year |
|---|---|
[Diagnostic image (117). A man with frequent blood transfusion and blister on his fingers. A form of porpheria cutanea tarda caused by excess iron].
Topics: Aged; Blister; Diagnosis, Differential; Enzyme Inhibitors; Humans; Hydroxyurea; Iron Chelating Agent | 2002 |