Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare disorder of porphyrin and heme metabolism characterized by infantile or childhood onset of severe cutaneous photosensitivity in affected males, presenting as tingling, burning, and itching within minutes of light exposure, often accompanied by swelling and redness of the skin. Pain may persist for hours or days after the initial reaction. Some patients show hepatic involvement and gallstone formation. Laboratory examination reveals increased levels of zinc- and metal-free protoporphyrin. The phenotype in heterozygous females ranges from asymptomatic to severe. Disease data Klasyfikacja Disease Synonimy X-linked dominant erythropoietic protoporphyria Dominująca protoporfiria erytropoetyczna sprzężona z chromosomem X Dominująca protoporfiria sprzężona z chromosomem X XLDPP XLP XLPP X-linked dominant protoporphyria XLDPP XLPP Kod ORPHA 443197 Kod OMIM 300752 Kod ICD10 E80.0 Kod ICD11 - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl