Familial porphyria cutanea tarda
MONDO:0008296An instance of porphyria cutanea tarda that is caused by an inherited modification of the individual's genome.
Also known as: hereditary porphyria cutanea tarda, porphyria cutanea tarda type II, porphyria cutanea tarda, susceptibility to, PCT, PCT, 'familial' type, PCT, type 2, Urod deficiency, porphyria cutanea tarda
3 clinical trials for this condition and its sub-types, 1 tagged with Familial porphyria cutanea tarda itself.
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A drop of blood, a faster answer: new test aims to outpace sepsis in preterm infants
Diagnosis Not yet recruitingThis pilot study is testing whether a rapid, point-of-care blood test can help identify early signs of infection and sepsis in preterm infants. Researchers will measure inflammatory markers like IL-6, PCT, CRP, and MxA in blood samples from about 40 to 80 premature babies, compar…
Sponsor: Medical University of Graz • Aim: Diagnosis
Last updated Aug 21, 2026 00:00 UTC
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Can immune fingerprints unlock new treatments for skin disease?
Knowledge-focused Not yet recruitingThis observational study aims to map the immune and molecular profiles of people with inflammatory skin conditions, including genetic forms like epidermolysis bullosa. By comparing these profiles to those of healthy individuals, researchers hope to identify unique signatures that…
Sponsor: Guy's and St Thomas' NHS Foundation Trust • Aim: Knowledge-focused
Last updated Aug 20, 2026 00:00 UTC