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Difference between revisions of "Peutz-Jeghers syndrome"
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Peutz-Jeghers syndrome (view source)
Revision as of 02:05, 27 September 2011
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'''Peutz-Jeghers syndrome''', abbreviated '''PJS''', is a constellation of findings inherited with an autosomal dominant pattern due to a defect in the STK11 gene. | '''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> | ||
==Clinical== | ==Clinical== | ||
Features:<ref> | Features:<ref name=omim175200>{{OMIM|175200}}</ref> | ||
*Melanocytic macules. | *Melanocytic macules. | ||
**Lips, buccal mucosa, and digits. | **Lips, buccal mucosa, and digits. | ||