Hamartoma Syndrome, Multiple


Bannayan Riley Ruvalcaba Syndrome

Bannayan Zonana Syndrome

Bannayan-Riley-Ruvalcaba Syndrome

Bannayan-Ruvalcaba-Riley Syndrome

Bannayan-Zonana Syndrome

Cerebellum Dysplastic Gangliocytoma

Cerebellum Dysplastic Gangliocytomas

Cowden Disease

Cowden Syndrome

Cowden's Disease

Cowden's Syndrome

Cowdens Disease

Cowdens Syndrome

Dysplastic Gangliocytoma of Cerebellum

Dysplastic Gangliocytoma of the Cerebellum

Hamartoma Syndromes, Multiple

Lhermitte Duclos Disease

Lhermitte-Duclos Disease

Macrocephaly, Multiple Lipomas, and Hemangiomata

Macrocephaly, Pseudopapilledema, and Multiple Hemangiomas

Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata

Multiple Hamartoma Syndrome

Multiple Hamartoma Syndromes

Myhre Riley Smith Syndrome

Myhre-Riley-Smith Syndrome

PTEN Hamartoma Tumor Syndrome

Riley Smith Syndrome

Riley-Smith Syndrome

Ruvalcaba Myhre Smith Syndrome

Ruvalcaba-Myhre Syndrome

Ruvalcaba-Myhre-Smith Syndrome

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.