X-linked erythropoietic protoporphyria

Orpha code: 443197OMIM code: 300752

Definition

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
Classification

Disease

Synonyms
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
ORPHA code
443197
OMIM code
300752
ICD10 code
E80.0
ICD11 code
-

No additional description.

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