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...
This page was last updated on October 11th, 2008
This page was last updated on October 11th, 2008
Cowden Syndrome (from Genetic Disorders)
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Cowden Syndrome
A CHORUS notecard document about this syndrome.
Emergency Medicine
A introduction of Cowden disease followed by an in depth report, including treatment, medication and follow up.
Cowdens Syndrome Support Group
Offers information and message boards for families and patients affected by the disease.
A CHORUS notecard document about this syndrome.
A introduction of Cowden disease followed by an in depth report, including treatment, medication and follow up.
Offers information and message boards for families and patients affected by the disease.
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