Familial adenomatous polyposis

Disease

Assess risk or confirm diagnosis of familial adenomatous polyposis (FAP) or attenuated FAP.

In patients with hamartomatous polyp(s) and findings suspicious for PTEN hamartoma tumor syndrome: aka Cowden syndrome and Bannayan-Riley-Ruvalcaba syndromes

In patients with hamartomatous polyp(s) and findings suspicious for Peutz-Jeghers syndroms.

In patients with hamartomatous polyp(s) and findings suspicious for Juvenile polyposis coli (JPC).

Rule out Lynch syndrome.

Rule out lynch syndrome.

Rule out gastrointestinal cancer and bleeding.

As an alternative and supportive to APC target mutation assay.

Alternative to specific markers. Good for diagnosis and therapy selection.

Differentiate MUYTH-associated polyposis.