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What is another word for Congenital Erythropoietic Porphyrias?

Pronunciation: [kənd͡ʒˈɛnɪtə͡l ˌɜːɹɪθɹˌɒpɔ͡ɪˈɛtɪk pɔːfˈɪɹi͡əz] (IPA)

Congenital Erythropoietic Porphyrias, also known as CEP, is a rare genetic disorder that affects the production of heme, a component of hemoglobin. Individuals with CEP experience photosensitivity, anemia, and porphyrin buildup in various organs. Several synonyms exist for this condition, such as Gunther disease, erythropoietic porphyria, and CEPD. These terms are often used interchangeably to reference the same disorder. The condition is caused by mutations in the uroporphyrinogen III synthase gene, leading to the impairment of heme production. While there is currently no cure for Congenital Erythropoietic Porphyrias, management includes avoiding sunlight exposure, receiving blood transfusions, and taking medications to alleviate symptoms.
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What are the opposite words for Congenital Erythropoietic Porphyrias?

Congenital Erythropoietic Porphyrias (CEP) is a rare metabolic disorder that affects the production of heme, which is essential for creating healthy red blood cells. There are no antonyms for this medical condition, but it can be treated with certain measures that can help alleviate symptoms such as phototherapy, blood transfusions, and bone marrow transplant. Individuals with CEP can lead normal lives with the right care and management strategies. It is essential to diagnose and treat this condition as early as possible to avoid complications such as skin damage, severe anemia, and liver problems.

What are the antonyms for Congenital erythropoietic porphyrias?

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