Difference between revisions of "Peutz-Jeghers syndrome"

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[[Image:Peutz-Jeghers_syndrome_polyp.jpg|thumb|300px | Peutz-Jeghers polyp, as may be seen in Peutz-Jeghers syndrome. (WC)]]
'''Peutz-Jeghers syndrome''', abbreviated '''PJS''', is a constellation of findings inherited with an autosomal dominant pattern due to a defect in the STK11 gene.<ref name=omim602216>{{OMIM|602216}}</ref>
'''Peutz-Jeghers syndrome''', abbreviated '''PJS''', is a constellation of findings inherited with an autosomal dominant pattern due to a defect in the STK11 gene.<ref name=omim602216>{{OMIM|602216}}</ref>


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