Jeghers-Peutz Syndrome
[An inherited condition characterized by generalized hamartomatous multiple polyposis of the intestinal tract. Transmitted in an autosomal dominant fashion, Peutz-Jeghers syndrome consistently involves the jejunum and is associated with melanin spots of the lips, buccal mucosa, and fingers. This syndrome is associated with abnormalities of chromosome 19. Also known as Jeghers-Peutz syndrome and Peutz's syndrome. —2004 ( NCI )]
UMLS (NCI) C0031269- Disease or Syndrome
Relation/PAR: Intestinal Polyps
Lentiginosis
Familiar Neoplastic Syndrome
Lentiginosis
Familiar Neoplastic Syndrome
Buy website
Medical Clinic. Optician. Pharmacy. Physician. Travel Agency. Hotel reservation. Child Care. Education. Teachers. Lessons. Tests and Exams. Certification. Shopping Center. Store. Real Estate.Affordable prices from $100.
  |
home
