Additional
Information: Cowden disease (CD), also termed Cowden syndrome and multiple hamartoma syndrome, is an autosomal dominant condition with variable expression that results from a mutation in the PTEN gene on chromosome arm 10q, as reported by Liaw et al. CD causes hamarto
Cowden Syndrome Sites:
Emergency Medicine Emergency Medicine: A introduction of Cowden disease followed by an in depth report, including treatment, medication and follow up. (Cowden Syndrome) http://emedicine.com/DERM/topic86.htm
Cowdens Syndrome Support Group Cowdens Syndrome Support Group: Offers information and message boards for families and patients affected by the disease. (Cowden Syndrome) http://groups.msn.com/cowdenssyndrome
Cowden Syndrome Cowden Syndrome: A CHORUS notecard document about this syndrome. (Cowden Syndrome) http://chorus.rad.mcw.edu/doc/00100.html