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O síndrome de Gorlin-Goltz, também conhecido como síndrome nevoide-basocelular, é uma doença genética rara caracterizada pela presença de múltiplos tumores na pele, anomalias esqueléticas, quistos na mandíbula e outras manifestações. É causado por mutações no gene PTCH1, que está envolvido na via de sinalização Hedgehog.
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