Familial porphyria cutanea tarda

MONDO:0008296

An 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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Including sub-types (3) Tagged with Familial porphyria cutanea tarda (1)

Not yet recruiting 1

A drop of blood, a faster answer: new test aims to outpace sepsis in preterm infants

Diagnosis Not yet recruiting

This 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

Familial porphyria cutanea tarda

Where it sits in the disease tree

A drop of blood, a faster answer: new test aims to outpace sepsis in preterm infants