| Cowden d. |
an autosomal dominant disorder comprising a combination of ectodermal, mesodermal, and endodermal anomalies, characterized by development of multiple hamartomatous lesions, especially in the skin, oral mucosa, breast, thyroid, colon, and intestines, and associated with a high incidence of malignancies in the organs involved. Called also multiple hamartoma syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
|---|---|
| Cowden disease |
see under disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|