Erythropoietic protoporphyria (Q66840): Difference between revisions
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A protoporfiria eritropoiética é um distúrbio hereditário da via metabólica do heme, caracterizado pelo acúmulo de protoporfirina no sangue, eritrócitos e tecidos, e manifestações cutâneas de fotossensibilidade. | |||
| description / en | description / en | ||
Erythropoietic protoporphyria (EPP) is an inherited disorder of the heme metabolic pathway characterised by accumulation of protoporphyrin in blood, erythrocytes and tissues, and cutaneous manifestations of photosensitivity. | |||
Revision as of 14:40, 14 August 2026
Erythropoietic protoporphyria (EPP) is an inherited disorder of the heme metabolic pathway characterised by accumulation of protoporphyrin in blood, erythrocytes and tissues, and cutaneous manifestations of photosensitivity.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1642941362 |
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| English | Erythropoietic protoporphyria |
Erythropoietic protoporphyria (EPP) is an inherited disorder of the heme metabolic pathway characterised by accumulation of protoporphyrin in blood, erythrocytes and tissues, and cutaneous manifestations of photosensitivity. |
