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Peutz-Jeghers Syndrome

"Peutz-Jeghers Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

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A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits.


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This graph shows the total number of publications written about "Peutz-Jeghers Syndrome" by people in UAMS Profiles by year, and whether "Peutz-Jeghers Syndrome" was a major or minor topic of these publications.
Bar chart showing 1 publications over 1 distinct years, with a maximum of 1 publications in 2013
To see the data from this visualization as text, click here.
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