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categorized as sporadic.
Familial adenomatous polyposis Peutz–Jeghers
syndrome Turcot syndrome Juvenile polyposis syndrome Cowden disease Bannayan–Riley–Ruvalcaba...
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Gardner syndrome,
familial polyposis of the colon, or
familial colorectal polyposis) is a
subtype of
familial adenomatous polyposis (FAP).
Gardner syndrome...
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third variant,
autosomal recessive familial adenomatous polyposis or MUTYH-****ociated
polyposis, is also
milder and, as its name suggests,
requires both...
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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...
- MUTYH-****ociated
polyposis (also
known as MYH-****ociated
polyposis) is an
autosomal recessive polyposis syndrome. The
disorder is
caused by
mutations in...
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Serrated polyposis syndrome (SPS),
previously known as
hyperplastic polyposis syndrome, is a
disorder characterized by the
appearance of
serrated polyps...
- 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...
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classed as one of
various hereditary intestinal polyposis syndromes and one of
various hamartomatous polyposis syndromes. It has an
incidence of approximately...
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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"....
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Polyposis registries exists for the
purpose of
understanding the
genetic disease familial adenomatous polyposis. The
registries provide a
service to doctors...
