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Association of hereditary spherocytosis with familial adenomatous polyposis in a pedigree: a new syndrome or coincidence?

✍ Scribed by Keiji Hirata; Kentaro Matsumoto; Kiyoshi Gondo; Kouichi Matsuzaki; Kazuhisa Akahane; Aiichiro Higure; Yoshifumi Nakayama; Kohji Okamoto; Tetsumi Konishi; Naoki Nagata; Hideaki Itoh

Publisher
Springer Japan
Year
2003
Tongue
English
Weight
136 KB
Volume
38
Category
Article
ISSN
0944-1174

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## BACKGROUND. Familial adenomatous polyposis (FAP) is a dominantly inherited disorder characterized by the presence of more than 100 adenomatous polyps in the colon and rectum starting in the second decade of life. FAP is associated with extra colonic manifestations, including desmoid tumors.