Familial non-medullary thyroid cancer in Iceland

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Familial non-medullary thyroid cancer: unraveling the genetic maze.

Familial non-medullary thyroid cancer (FNMTC) constitutes 3-9% of all thyroid cancers. Out of all FNMTC cases, only 5% in the syndromic form has well-studied driver germline mutations. These associated syndromes include Cowden syndrome, familial adenomatous polyposis, Gardner syndrome, Carney complex type 1, Werner syndrome and DICER1 syndrome. It is important for the clinician to recognize the...

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Medullary Thyroid Cancer: A Review

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Genetic and Epigenetic of Medullary Thyroid Cancer

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A dog pedigree with familial medullary thyroid cancer.

Multiple endocrine neoplasia (MEN) is defined as concurrent neoplasia or hyperplasia in more than one endocrine gland. MEN is well known in humans and has also been reported in small animals. We report on a dog family of a mixed breed with Alaskan malamute as a major influence, where three members developed thyroid carcinomas and another dog had clinical signs mimicking the other three but with...

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BACKGROUND Familial non-medullary thyroid cancer (fNMTC) is a complex genetic disorder that is more aggressive than its sporadic counterpart. Thus far, three genetic loci have been implicated in susceptibility to fNMTC by linkage analysis. METHODS We used linkage analysis to test the significance of two of the known susceptibility loci for fNMTC, TCO on 19p13 and NMTC1 on 2q21 in 10 fNMTC fam...

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ژورنال

عنوان ژورنال: Journal of Medical Genetics

سال: 2001

ISSN: 1468-6244

DOI: 10.1136/jmg.38.3.189