Login
Toggle sidebar

Lint: cowden-syndrome

cowden-syndrome
Emphasis
warning

"It carries an autosomal dominant inheritance with variable (but high) penetrance 7. A gene locus for the disease has been identified on chromosome 10q22-23, a mutation of the PTEN gene 7."

Line 41:193 · Italics should be used only in exceptional circumstances: '<em>PTEN</em>'

"Thus, Cowden syndrome is part of a group of disease known as PTEN-related diseases, which also includes 3,7:"

Line 42:68 · Italics should be used only in exceptional circumstances: '<em>PTEN</em>'
Biographical Lifespan
suggestion

"History and etymology"

Line 47:1 · A bold element in the History and etymology section should be a person; it would be useful to have their lifespan details: '<h4>History and etymology</h4> <p>First described in 1963 by K M Lloyd and M Dennis with the surname of their first patient: <strong>Cowden</strong> '
Links
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
1
6
2
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0