Infantile juvenile polyposis syndrome: A rare cause of protein-losing enteropathy

Infantile juvenile polyposis syndrome: A rare cause of protein-losing enteropathy

Juvenile Polyposis Syndrome (JPS) is a rare autosomal dominant hereditary syndrome affecting 1:100000-160000 individuals. JPS most presents with rectal bleeding, anemia, abdominal pain, obstruction and rarely with rectal prolapsus of the polyp. In this case, we diagnosed Infantile Juvenile Polyposis...

Full description

Bibliographic Details
Main Authors: Tufan Kutlu, Fugen Cullu, Sibel Erdamar, Tulay Erkan, Nuray Kepil, Faruk Beser, Didem Gülcü
Format: Article
Language:English
Published: Journal of Surgery and Medicine 2020-10-01
Series:Journal of Surgery and Medicine
Subjects:
rectal bleeding
infantile juvenile polyposis syndrome
protein lossing enteropaty
rektal kanama
i̇nfantil juvenil polipozis sendromu
protein kaybettiren enteropati
Online Access:https://dergipark.org.tr/en/pub/josam/issue/57049/729936

Internet

https://dergipark.org.tr/en/pub/josam/issue/57049/729936

Similar Items