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Conheça mais sobre a doença da Fenilcetonúria A Fenilcetonúria é uma condição congênita hereditária rara que causa acúmulo do aminoácido fenilalanina no corpo. Os sintomas mais comuns são: vômitos, inflamações na pele, odor característico na urina, microcefalia, convulsões, hipertonia muscular, hiperatividade, atraso do crescimento, dificuldade para firmar a cabeça e se sentar. O diagnóstico precoce é possível através do teste do pezinho. E aqui vai uma curiosidade: o método da triagem neonatal
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Pessoas com fenilcetonúria, uma doença hereditária que leva ao acúmulo de fenilalanina no sangue, devem evitar o consumo de spirulina, assim como pessoas com doenças autoimunes, gestantes e lactantes.
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