What is another word for Congenital Erythropoietic Porphyria?
Pronunciation: [kənd͡ʒˈɛnɪtə͡l ˌɜːɹɪθɹˌɒpɔ͡ɪˈɛtɪk pɔːfˈɪɹi͡ə] (IPA) 
Congenital Erythropoietic Porphyria (CEP) is a rare genetic disorder that affects the production of heme, a component of hemoglobin. Also known as Günther's disease, CEP is characterized by skin sensitivity to sunlight and anemia. Synonyms for CEP include erythropoietic porphyria, congenital erythropoietic porphyria, and erythropoietic protoporphyria. While erythropoietic porphyria and erythropoietic protoporphyria may refer to different types of porphyria, these terms have been used interchangeably in the past. Regardless of the specific terminology, CEP is a challenging condition to manage, with treatments aimed at alleviating symptoms and preventing complications.
