Peutz-Jeghers Syndrome without Polyposis
Peutz-Jeghers syndrome is generally considered a condition in which familial gastrointestinal polyposis is associated with a characteristic pigmentation of the skin and mucous membranes Two members of a family in which the characteristic pigmentation was present in the absence of gastrointestinal po...
Saved in:
Main Authors: | Anthony G. Catto-Smith, Mark K. Patrick, D. Grant Gall |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
1988-01-01
|
Series: | Canadian Journal of Gastroenterology |
Online Access: | http://dx.doi.org/10.1155/1988/451742 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Large Rearrangements in Genes Responsible for Familial Adenomatous Polyposis, <i>MUTYH</i>-Associated Polyposis and Peutz–Jeghers Syndrome in Russian Patients
by: A. N. Loginova, et al.
Published: (2023-06-01) -
Peutz–Jeghers syndrome: review of the literature and clinical case presentation
by: V. O. Kaybysheva, et al.
Published: (2011-03-01) -
Childhood Peutz-Jeghers Syndrome: Diversity of Clinical Features and Complications, and Literature Review
by: Mark R Oliver, et al.
Published: (1994-01-01) -
Asymptomatic Gastric Giant Polyp in a Boy with Peutz-Jeghers Syndrome Presented with Multiple Café Au Lait Traits
by: Christos Plataras, et al.
Published: (2018-01-01) -
Sorbitol as a Cryptic Cause of Diarrhea
by: Anthony G. Catto-Smith, et al.
Published: (1988-01-01)