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...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Journal of Surgery and Medicine
2020-10-01
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Series: | Journal of Surgery and Medicine |
Subjects: | |
Online Access: | https://dergipark.org.tr/en/pub/josam/issue/57049/729936 |