Syndrome

Hamartoma Syndrome, Multiple

AMW:DIS:040042

A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE.

Pathology clinical

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Hamartoma Syndrome, Multiple has parent Hamartoma

Proteus Syndrome has parent Hamartoma Syndrome, Multiple

Hamartoma Syndrome, Multiple has parent Neoplasms, Multiple Primary

Hamartoma Syndrome, Multiple has parent Neoplastic Syndromes, Hereditary

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