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Peutzov-Jeghersov syndróm

  1. Subject h.Peutzov-Jeghersov syndróm
    Subject h.Peutz-Jeghers Syndrome
    Entry termslentiginopolyposis digestiva
    lentiginóza periorálna
    Peutzov-Tourainov syndróm
    English X referencesLentiginosis, Perioral
    Scope note in EnglishA 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.
    Links (12) - ARTICLES
    (1) - CiBaMed
    (4) - BOOKS
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Number of the records: 1  

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