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Difference between revisions of "Peutz-Jeghers syndrome"
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Peutz-Jeghers syndrome (view source)
Revision as of 02:02, 27 September 2011
, 02:02, 27 September 2011+abbrev.
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'''Peutz-Jeghers syndrome''' 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. | ||
==Clinical== | ==Clinical== | ||