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dana farber genital melanotic macules Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant genetic disorder most often caused by mutations in the STK11 (LKB1) tumor suppressor gene. The condition is characterized by two hallmark features: hamartomatous polyps

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dana farber genital melanotic macules Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant genetic disorder most often caused by mutations in the STK11 (LKB1) tumor suppressor gene. The condition is characterized by two hallmark features: hamartomatous polyps

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dana farber genital melanotic macules Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant genetic disorder most often caused by mutations in the STK11 (LKB1) tumor suppressor gene. The condition is characterized by two hallmark features: hamartomatous polyps

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dana farber genital melanotic macules Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant genetic disorder most often caused by mutations in the STK11 (LKB1) tumor suppressor gene. The condition is characterized by two hallmark features: hamartomatous polyps

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dana farber genital melanotic macules Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant genetic disorder most often caused by mutations in the STK11 (LKB1) tumor suppressor gene. The condition is characterized by two hallmark features: hamartomatous polyps

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dana farber genital melanotic macules Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant genetic disorder most often caused by mutations in the STK11 (LKB1) tumor suppressor gene. The condition is characterized by two hallmark features: hamartomatous polyps
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