Top/Health/Conditions and Diseases/Genetic Disorders/Cowden Syndrome
Cowden Syndrome :
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 hamartomatous neoplasms of the skin and mucosa, GI tract, bones, central nervous system (CNS), eyes, and genitourinary tract. Skin is involved in 90-100% of cases; the thyroid in 66%.
3 web sites matced for Cowden Syndrome
Emergency Medicine
A introduction of Cowden disease followed by an in depth report, including treatment, medication and follow up.
Cowden Syndrome
A CHORUS notecard document about this syndrome.
Cowdens Syndrome Support Group
Offers information and message boards for families and patients affected by the disease.
 
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