Hereditary photodermatosis
MONDO:0015951Hereditary photodermatoses are a spectrum of rare photosensitive disorders that are often caused by genetic deficiency or malfunction of various components of the DNA repair pathway. This results clinically in extreme photosensitivity, with many syndromes exhibiting an increased risk of cutaneous malignancies.
Also known as: photogenodermatosis, photogénodermatose, genetic photosensitivity, genetic skin photosensitivity
33 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Erythropoietic protoporphyria
(13)
X-linked erythropoietic protoporphyria
(9)
Hereditary coproporphyria
(5)
Acute intermittent porphyria
(4)
Xeroderma pigmentosum
(3)
Cutaneous porphyria
(2)
Protoporphyria, erythropoietic, 1
(2)
Variegate porphyria
(2)
Rothmund-Thomson syndrome
(1)
Xeroderma pigmentosum-Cockayne syndrome complex
(1)
Xeroderma pigmentosum group F
(1)
Xeroderma pigmentosum variant type
(1)
Autosomal erythropoietic protoporphyria
(0)
Bloom syndrome
(0)
Chester porphyria
(0)
CPOX-related hereditary coproporphyria
(0)
Encephalopathy, porphyria-related
(0)
Erythropoietic uroporphyria associated with myeloid malignancy
(0)
Familial porphyria cutanea tarda
(0)
Harderoporphyria
(0)