The risk of gastrointestinal carcinoma in familial juvenile polyposis

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

1975 ◽  
Vol 83 (5) ◽  
pp. 639 ◽  
Author(s):  
THOMAS J. STEMPER


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 ◽  
...  


The Lancet ◽  
1982 ◽  
Vol 319 (8263) ◽  
pp. 68-71 ◽  
Author(s):  
J.M. Müller ◽  
C. Dienst ◽  
U. Brenner ◽  
H. Pichlmaier


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


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