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. 2012 May 3;3:61. doi: 10.3389/fendo.2012.00061

Table 1.

Hereditary tumor syndromes associated with thyroid cancer.

Disease Histological type Gene mutation Location Incidence of thyroid cancer Pathological variant of PTC
FAP and Gardner syndrome PTC APC tumor suppressor gene 5q21 2–12% Cribriform-morular classical variant
Cowden syndrome FTC, PTC, C-cell hyperplasia PTEN tumor suppressor gene 10q23.2 >10%
Carney complex FTC, PTC PRKAR1-x 2p16 17q22–24 60 and 4%
Werner syndrome FTC, PTC, ATC WRN gene 8p11–p12 18%

PTC, papillary thyroid cancer; FAP, familial adenomatous polyposis; APC, adenomatous polyposis coli; FTC, follicular thyroid cancer; PTEN, phosphatase and tensin; PRKAR1-x protein kinase A regulatory subunit type 1-alpha; ATC, anaplastic thyroid cancer; WRN, Werner.