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La fibrosi cistica è una malattia genetica grave con un’incidenza in Italia di circa un neonato su 3000. Il bambino nasce malato quando entrambi i genitori sono portatori sani di una mutazione del gene CFTR ed entrambi la trasmettono al figlio. Il test del portatore sano permette d’identificare le mutazioni del gene CFTR che causano la fibrosi cistica e stabilire così nel singolo o nella coppia il rischio di avere figli malati: è consigliato in particolare per chi ha parenti affetti dalla malatt
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La fibrosi cistica è una malattia genetica grave con un’incidenza i…
46.2K viewsApr 11, 2024
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