Number of the records: 1  

Peutzov-Jeghersov syndróm

  1. Record numberd010580
    Date06.06.2025
    TypeM
    Topical termPeutzov-Jeghersov syndróm
    Other termEnglish (Pseudonym) Lentiginosis, Perioral
    Slovak (Pseudonym) lentiginopolyposis digestiva
    Slovak (Pseudonym) lentiginóza periorálna
    Slovak (Pseudonym) Peutzov-Tourainov syndróm
    UDCC04.700.633C06.405.469.578.750C16.320.700.667C17.800.621.430.530.550.625
    NoteA 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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Number of the records: 1  

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