Cowden syndrome is a very rare genetic disease classically manifesting as the appearance of multiple hamartomas – a benign (but still problematic) kind of tumor – both on the skin and within internal organs.
Cowden syndrome is a very rare genetic disease classically manifesting as the appearance of multiple hamartomas – a benign (but still problematic) kind of tumor – both on the skin and within internal organs.
[gravityform id="8" name="Contact Form" description="false"]