Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Non-medullary thyroid cancer 3

Hereditary non-medullary thyroid cancer 3 is an autosomal dominant disorder caused by mutations in the chromosomal region 2q21.

Systematic

Non-medullary thyroid cancer
Familial follicular thyroid carcinoma
Follicular thyroid carcinoma
Hyperfunctioning thyroid adenoma
Non-medullary thyroid cancer 2
Non-medullary thyroid cancer 3
Non-medullary thyroid cancer 4
Non-medullary thyroid cancer 4
Non-medullary thyroid cancer 5
Thyroid carcinoma with thyrotoxicosis

References:

1.

Burgess JR et. al. (1997) Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid.

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2.

Vriens MR et. al. (2009) Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer.

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3.

McKay JD et. al. (1999) At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family.

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4.

McKay JD et. al. (2001) Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21.

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Update: Sept. 26, 2018