Number of the records: 1
syndróm mnohopočetného hamartómu
Record number d006223 Date 06.06.2025 Type M - MESH Topical term syndróm mnohopočetného hamartómu Other term English (Pseudonym) Bannayan-Riley-Ruvalcaba Syndrome
English (Pseudonym) Cowden Disease
English (Pseudonym) Cowden's Disease
English (Pseudonym) Lhermitte-Duclos Disease
English (Pseudonym) Multiple Hamartoma Syndrome
English (Pseudonym) PTEN Hamartoma Tumor Syndrome
Slovak (Pseudonym) Bannayanov-Rileyov-Ruvalcabov syndróm
Slovak (Pseudonym) Bannayanov-Zonanov syndróm
Slovak (Pseudonym) Cowdenova choroba
Slovak (Pseudonym) Cowdenov syndróm
Slovak (Pseudonym) gangliocytóm mozočka, dysplastický
Slovak (Pseudonym) Lhermitte-Duclosova choroba
Slovak (Pseudonym) L'Hermitte-Duclosova choroba
Slovak (Pseudonym) makrocefália, mnohopočetné lipómy a menangiómy
Slovak (Pseudonym) makrocefália, pseudopapiloedém a mnohopočetné hemangiómy
Slovak (Pseudonym) Myhreov-Rileyov-Smithov syndróm
Slovak (Pseudonym) syndróm s PTEN hamartómami
Slovak (Pseudonym) Rileyov-Smithov syndróm
Slovak (Pseudonym) Ruvalcabov-Myhreov syndróm
UDC C04.445.435C04.651.435C04.700.435C16.320.700.435 Note 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. 
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Number of the records: 1