Peutz-Jeghers Syndrome
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.
推出的年份: 1965
树号: C04.700.633, C06.405.469.578.750, C16.320.700.667, C17.800.621.430.530.550.625
MeSH 单一 ID: D010580
进入的组:
Peutz Jeghers Syndrome
Syndrome, Peutz-Jeghers
Polyposis, Hamartomatous Intestinal
Hamartomatous Intestinal Polyposes
Hamartomatous Intestinal Polyposis
Intestinal Polyposes, Hamartomatous
Intestinal Polyposis, Hamartomatous
Polyposes, Hamartomatous Intestinal
Peutz-Jegher's Syndrome
Peutz Jegher's Syndrome
Peutz-Jegher Syndrome
Syndrome, Peutz-Jegher's
Peutz-Jeghers Polyposis
Peutz Jeghers Polyposis
Polyposis, Peutz-Jeghers
Periorificial Lentiginosis Syndrome
Periorificial Lentiginosis Syndromes
Syndrome, Periorificial Lentiginosis
Syndromes, Periorificial Lentiginosis
Lentiginosis, Perioral
Lentiginoses, Perioral
Perioral Lentiginoses
Perioral Lentiginosis
Polyps-and-Spots Syndrome
Polyps and Spots Syndrome
Polyps-and-Spots Syndromes
Syndrome, Polyps-and-Spots
Syndromes, Polyps-and-Spots
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