-
categorized as sporadic.
Familial adenomatous polyposis Peutz–Jeghers
syndrome Turcot syndrome Juvenile polyposis syndrome Cowden disease Bannayan–Riley–Ruvalcaba...
-
third variant,
autosomal recessive familial adenomatous polyposis or MUTYH-****ociated
polyposis, is also
milder and, as its name suggests,
requires both...
-
Gardner syndrome,
familial polyposis of the colon, or
familial colorectal polyposis) is a
subtype of
familial adenomatous polyposis (FAP).
Gardner syndrome...
-
Adenomatous polyposis coli (APC) also
known as
deleted in
polyposis 2.5 (DP2.5) is a
protein that in
humans is
encoded by the APC gene. The APC protein...
-
nasal polyposis. In
people with
cystic fibrosis,
nasal polyps are
noted in 37% to 48%. Newton, JR; Ah-See, KW (April 2008). "A
review of
nasal polyposis"....
-
classed as one of
various hereditary intestinal polyposis syndromes and one of
various hamartomatous polyposis syndromes. It has an
incidence of approximately...
-
Serrated polyposis syndrome (SPS),
previously known as
hyperplastic polyposis syndrome, is a
disorder characterized by the
appearance of
serrated polyps...
- cancer. Its
histology is
usually adenocarcinoma.
Familial adenomatous polyposis (FAP),
Gardner syndrome,
Lynch syndrome, Muir–Torre syndrome,
celiac disease...
- a
family history of
juvenile polyposis. Age of
onset is variable. The term 'juvenile' in the
title of
juvenile polyposis syndrome refers to the histological...
-
conditions include Lynch-like syndrome,
polymerase proofreading-****ociated
polyposis and
familial colorectal cancer type X.
Lifetime risk and mean age at diagnosis...
