general_pathology:neoplasia:neoplasia_50
Choose the correct answer
Cowden syndrome is an autosomal dominant mutation of which tumour suppressor gene?
”Explanation”
Cowden Syndrome is a condition marked by frequent benign growths such as skin appendages and an increased risk of epithelial cancers (breast, thyroid and endometrium). PTEN inhibits the PI3K/Atk signalling cascade.
general_pathology/neoplasia/neoplasia_50.txt · Last modified: by achamings