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  2. Erythropoietic porphyria - Wikipedia

    en.wikipedia.org/wiki/Erythropoietic_porphyria

    X-linked dominant erythropoietic protoporphyria is a relatively mild version of porphyria with the predominant symptom being extreme photosensitivity causing severe itching and burning sensation of the skin due to the buildup of protoporphyrin IX. One possible treatment was discovered when treating an individual with supplemental iron for a ...

  3. Gunther disease - Wikipedia

    en.wikipedia.org/wiki/Gunther_disease

    Günther disease is a congenital form of erythropoietic porphyria.The word porphyria originated from the Greek word porphura. Porphura actually means "purple pigment", which, in suggestion, the color that the body fluid changes when a person has Gunther's disease. [3]

  4. Photosensitivity in animals - Wikipedia

    en.wikipedia.org/wiki/Photosensitivity_in_animals

    A common condition seen in animals is congenital porphyria due to the accumulation of Uroporphyrin, which is deposited in the teeth and bones, giving them a pink discolouration, or excreted through the urine, exhibiting a pinkish fluorescence under ultraviolet light.

  5. Erythropoietic protoporphyria - Wikipedia

    en.wikipedia.org/wiki/Erythropoietic_protoporphyria

    Erythropoietic protoporphyria (or commonly called EPP) is a form of porphyria, which varies in severity and can be very painful. It arises from a deficiency in the enzyme ferrochelatase , leading to abnormally high levels of protoporphyrin in the red blood cells (erythrocytes) , plasma, skin, and liver . [ 2 ]

  6. Uroporphyrinogen III synthase - Wikipedia

    en.wikipedia.org/wiki/Uroporphyrinogen_III_synthase

    Uroporphyrinogen III synthase (EC 4.2.1.75) is an enzyme involved in the metabolism of the cyclic tetrapyrrole compound porphyrin.It is involved in the conversion of hydroxymethyl bilane into uroporphyrinogen III.

  7. Porphyria - Wikipedia

    en.wikipedia.org/wiki/Porphyria

    The rarest is congenital erythropoietic porphyria (CEP), otherwise known as Gunther's disease. The signs may present from birth and include severe photosensitivity, brown teeth that fluoresce in ultraviolet light due to deposition of Type 1 porphyrins, and later hypertrichosis. Hemolytic anemia usually develops.

  8. Category:Porphyrias - Wikipedia

    en.wikipedia.org/wiki/Category:Porphyrias

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  9. Protoporphyrinogen oxidase - Wikipedia

    en.wikipedia.org/wiki/Protoporphyrinogen_oxidase

    Variegate porphyria is caused by mutations in the PPOX gene. More than 100 mutations that can cause variegate porphyria have been identified in the PPOX gene. One mutation, a substitution of the amino acid tryptophan for arginine at position 59 (also written as Arg59Trp or R59W), is found in about 95 percent of South African families with variegate porphyria.