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Erythropoietic Protoporphyria in Latin America

July 8, 2021
LatM INsight
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Porphyrias are a group of diseases due to an alteration in the metabolism of porphyrins, which generates an increase in the accumulation and excretion of their intermediate chemicals. They can be classified according to their main manifestations as cutaneous, acute, or mixed, or by the location where the enzymatic deficiency predominates, as hepatic or erythropoietic.

Erythropoietic Protoporphyria in Latin America

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enzymedeficiency EPP ferrochelatase latinamerica latm latminsight porphyrin raredisease
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#huntersyndrome #Iduronate2sulfatasedeficiency #latinaamerica #mucopolysaccharidosisII brazil Casa Hunter Enzyme deficiency enzymedeficiency EPP ferrochelatase genetic disorders Hunter syndrome Iduronate Sulfatase Instituto de Genética para Todos latinamerica Latin America latm latminsight Lysosomal enzyme deficiencies Lysosome MPS type II Mucopolysaccharidosis porphyrin raredisease Rare Diseases

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