lamotrigine has been researched along with Coproporphyria, Hereditary in 1 studies
Coproporphyria, Hereditary: An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, 5-AMINOLEVULINATE and COPROPORPHYRINS.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Ms F's hereditary coproporphyria was diagnosed 9 years before the current admission." | 2.50 | Lamotrigine in the treatment of psychotic depression associated with hereditary coproporphyria -- case report and a brief review of the literature. ( Gazdag, G; Kassai-Farkas, Á; Makkos, Z; Pusztai, Á; Takács, R; Ungvári, GS, 2014) |
| 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 |
|---|---|
| Takács, R | 1 |
| Makkos, Z | 1 |
| Kassai-Farkas, Á | 1 |
| Pusztai, Á | 1 |
| Ungvári, GS | 1 |
| Gazdag, G | 1 |
1 review available for lamotrigine and Coproporphyria, Hereditary
| Article | Year |
|---|---|
Lamotrigine in the treatment of psychotic depression associated with hereditary coproporphyria -- case report and a brief review of the literature.
Topics: Adult; Antipsychotic Agents; Coproporphyria, Hereditary; Depressive Disorder, Major; Female; Humans; | 2014 |