Juvenile polyposis-a precancerous condition

2007 ◽  
Vol 13 (6) ◽  
pp. 619-630 ◽  
Author(s):  
J. R. JASS ◽  
C. B. WILLIAMS ◽  
H. J. R. BUSSEY ◽  
B. C. MORSON
2020 ◽  
Vol 13 (12) ◽  
pp. e236855
Author(s):  
Wendy Chang ◽  
Patricia Renaut ◽  
Casper Pretorius

Juvenile polyposis syndrome (JPS) and hereditary haemorrhagic telangiectasia (HHT) are rare autosomal dominant diseases, where symptoms manifest at childhood. A 32-year-old man with no family history of JPS or HHT with SMAD4 gene mutation who developed signs and symptoms only at the age of 32, when he was an adult. In this article, we highlight the steps taken to diagnose this rare pathology, explain its pathophysiology and management.


2001 ◽  
Vol 69 (4) ◽  
pp. 704-711 ◽  
Author(s):  
Xiao-Ping Zhou ◽  
Kelly Woodford-Richens ◽  
Rainer Lehtonen ◽  
Keisuke Kurose ◽  
Micheala Aldred ◽  
...  

1967 ◽  
Vol 63 (sup224) ◽  
pp. 15-15 ◽  
Author(s):  
J. J. Pindborg

2021 ◽  
Vol 51 ◽  
pp. 101901
Author(s):  
Blain Murphy ◽  
Charlene M. McShane ◽  
Olinda Santin ◽  
Charlene Treanor ◽  
Bronagh Byrne ◽  
...  

1998 ◽  
Vol 5 (8) ◽  
pp. 751-756 ◽  
Author(s):  
James R. Howe ◽  
Frank A. Mitros ◽  
Robert W. Summers

2012 ◽  
Vol 55 (8) ◽  
pp. 886-892 ◽  
Author(s):  
Margaret O’Malley ◽  
Lisa LaGuardia ◽  
Matthew F. Kalady ◽  
Joseph Parambil ◽  
Brandie Heald ◽  
...  

1990 ◽  
Vol 33 (11) ◽  
pp. 980-984 ◽  
Author(s):  
Walter E. Longo ◽  
Robert J. Touloukian ◽  
Brian A. West ◽  
Garth H. Ballantyne

2011 ◽  
Vol 148 (1) ◽  
pp. 64-66 ◽  
Author(s):  
A. Elhjouji ◽  
A. Aitali ◽  
F. Rouibaa ◽  
I. Rharrassi ◽  
A. Zentar ◽  
...  

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