Porphyria cutanea tarda |
Familial PCT; PCT; UROD deficiency; Uroporphyrinogen decarboxylase deficiency |
Porphyria cutanea tarda is the most common type of porphyria. The disorder results from low levels of the enzyme responsible for the fifth step in heme production. Heme is a vital molecule for all of the body's organs. It is a component of hemoglobin, the molecule that carries oxygen in the blood. Porphyria cutanea tarda is a subtype of porphyria. When signs and symptoms occur, they usually begin in adulthood and result from the skin becoming overly sensitive to sunlight. Areas of skin expo ...
Wikipedia - [full article]
Porphyria cutanea tarda Clinical Trials
- Study of the Pathogenesis of Porphyria Cutanea Tarda
ClinicalTrials.gov Identifier: NCT00005103 - Completed
Porphyria Cutanea Tarda
- Risk Factors of Porphyria Cutanea Tarda (PCT)
ClinicalTrials.gov Identifier: NCT00213772 - Completed
Porphyria Cutanea Tarda
- Studies in Porphyria I: Characterization of Enzyme Defects
ClinicalTrials.gov Identifier: NCT00004331 - Recruiting
Porphyria
- Study of Nutritional Factors in Porphyria
ClinicalTrials.gov Identifier: NCT00004788 - Completed
Porphyria
- Studies in Porphyria IV: Gonadotropin-Releasing Hormone (GnRH) Analogues for Prevention of Cyclic Attacks
ClinicalTrials.gov Identifier: NCT00004330 - Completed
Porphyria
- Studies in Porphyria III: Heme and Tin Mesoporphyrin in Acute Porphyrias
ClinicalTrials.gov Identifier: NCT00004396 - Completed
Porphyria
- Phase I Study of Tin Mesoporphyrin in Patients on Long Term Heme Therapy for Prevention of Acute Attacks of Porphyria
ClinicalTrials.gov Identifier: NCT00004397 - Completed
Porphyria
- Phase I Study of Heme Arginate With or Without Tin Mesoporphyrin in Patients With Acute Attacks of Porphyria
ClinicalTrials.gov Identifier: NCT00004398 - Completed
Porphyria
- Phase I/II Study of Heme Arginate and Tin Mesoporphyrin for Acute Porphyria
ClinicalTrials.gov Identifier: NCT00004789 - Completed
Porphyria
- Diagnostic and Screening Study of Genetic Disorders
ClinicalTrials.gov Identifier: NCT00006057 - Completed
Tay-Sachs Disease; Porphyria, Erythropoietic; Leukodystrophy, Globoid Cell; Metabolism, Inborn Errors
- Porphozym in the Treatment of Acute Attacks in AIP
ClinicalTrials.gov Identifier: NCT00418795 - Completed
Acute Intermittent Porphyria

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