Genetic and environmental factors in the aetiology of simple goiter

References

• Studer H, Ramelli F. Simple goiter and its variants: Euthyroid 12. and hyperthyroid multinodular goiters. Endocr Rev 1982; 3: 40–61
   PubMedGoogle Scholar
• Wang C, Crapo L M. The epidemiology of thyroid disease and implications for screening. Endocrinol Metab Clin North Am 1997; 26: 189–218
   PubMed Web of Science ®Google Scholar
• Hennemann G, Krenning E P. Etiology of sporadic goitre. Treatment of endemic and sporadic goitre: International Thyroid Symposium, October 28–21, 1984, Budapest, D Reinwein, P C Scriba. Schattauer, StuttgartGermany 1985; 61–4
   Google Scholar
• Hegedüs L. Thyroid size determined by ultrasound. Influence 15. of physiological factors and non-thyroidal disease. Dan Med Bull 1990; 37: 249–63
   PubMedGoogle Scholar
• Orenstein H, Peskind A, Raskind M A. Thyroid disorders in female psychiatric patients with panic disorder or agoraphobia. Am J Psychiatry 1988; 145: 1428–30
   PubMed Web of Science ®Google Scholar
• Bertelsen J B, Hegedüs L. Cigarette smoking and the thyroid. Thyroid 1994; 4: 327–31
   PubMed Web of Science ®Google Scholar
• Bartels E D. Heredity in Graves' disease. Copenhagen 1941, With remarks on heredity in toxic adenoma in the thyroid, non-toxic goitre, and myxoedema [dissertation]. Copenhagen; University of 18
   Google Scholar
• Martin L, Fisher R A. The hereditary and familial aspects of exophtalmic goitre and nodular goitre. QJM 1945; 14: 207–19
   PubMedGoogle Scholar
• Malamos B, Koutras D A, Kostamis P, Kralios A C, Rigopoulos G, Zerefos N S. Endemic goiter in Greece: Epidemiologic and genetic studies. J Clin Endocrinol Metab 1966; 26: 688–95
   PubMedGoogle Scholar
• Allahabadia A, Nithiyananthan R, Franklyn J A, Gough S CL (1999) Genetic susceptibility to the development of sporadic non-toxic goiter. The Proceedings of the 72nd Annual Meeting of the American Thyroid Association, Palm Beach, FLUSA, Sep 29 - Oct 3, 1999. The American Thyroid Association, New York, NY, Abstract 49
   Google Scholar
• Couch R M, Hughes I A, De Sa D J, Schiffrin A, Guyda H, Winter J SD. An autosomal dominant form of adolescent multinodular goiter. Am J Hum Genet 1986; 39: 811–6
   PubMedGoogle Scholar
• Corral J, Martin C, Perez R, Sanchez I, Mories M T, San Millan J L, et al. Thyroglobulin gene point mutation associated with non-endemic simple goitre. Lancet 1993; 341: 462–4
   PubMedGoogle Scholar
• Bignell G R, Canzian F, Shayeghi M, Stark M, Shugart Y Y, Biggs P, et al. Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer. Am J Hum Genet 1997; 61: 1123–30
   PubMedGoogle Scholar
• Hawkes C H. Twin studies in medicine - what do they tell us. QJM 1997; 90: 311–21
   PubMedGoogle Scholar
• Greig W R, Boyle J A, Duncan A, Nicol J, Gray M J, Buchanan W W, et al. Genetic and non-genetic factors in simple goitre formation: evidence from a twin study. QJM 1967; 36: 175–88
   PubMedGoogle Scholar
• Malamos B, Koutras D A, Kostamis P, Rigopoulos G A, Zerefos N S, Yataganas X A. Endemic goitre in Greece: a study of 379 twin pairs. J Med Genet 1967; 4: 16–8
   PubMedGoogle Scholar
• Brix T H, Kyvik K O, Hegedüs L. Major role of genes in the etiology of simple goiter in females: a population-based twin study. J Clin Endocrinol Metab 1999; 84: 3071–5
   PubMedGoogle Scholar
• Brix T H, Hansen P S, Kyvik K O, Hegedüs L. Cigarette smoking and risk of clinically overt thyroid disease - a population based twin case-control study. Arch Intern Med 2000; 160: 661–6
   PubMedGoogle Scholar
• Neumann S, Wdgerodt H, Ackermann F, Reske A, Jung M, Reis A, et al. Linkage of familial euthyroid goiter to the multinodular goiter-1 locus and exclusion of the candidate genes thyroglobulin, thyroperoxidase, and Na+I− symporter. J Clin Endocrinol Metab 1999; 84: 3750–6
   PubMedGoogle Scholar
• McKay J D, Williamson J, Lesueur F, Stark M, Duffield A, Canzian F, et al. At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family. Eur J Endocrinol 1999; 141: 122–5
   PubMed Web of Science ®Google Scholar
• Tomer Y, Barbesino G, Keddache M, Greenberg D A, Davies T F. Mapping of a major susceptibility locus for Graves' disease (GD-1) to chromosome 14q31. J Clin Endocrinol Metab 1997; 82: 1645–8
   PubMed Web of Science ®Google Scholar