Hamartoma Syndrome, Multiple
| Medical Definition: |
A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Papules of the face and oral mucosa are the most characteristic lesion. Other changes occur in the skin, in the thyroid, the breast, the gastrointestinal system, and the nervous system. |
| Guide Notes: |
do not use /blood supply /chem /second /secret /ultrastruct |
| Previously Indexed: |
Hamartoma (1966-1986),Neoplasms, Multiple Primary (1966-1986) |
Hamartoma Syndrome, Multiple Medical Definitions and Terms
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 CANADIAN
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