Localized attachment loss in pendred syndrome: Incidental?

Journal of Periodontology

Volumn 78, Issue 5, 2007, Pages 948-954

  Dileep Sharma, C G ^a,b,c   Pradeep, A R ^b  

^a Kolar Gold Fields College of Dental Sciences   (India)

^b Government Dental College and Hospital   (India)

^c NONE   (India)

Author keywords

Autosomal recessive; Goiter; Hypercementosis; Hypothyroidism; Periodontitis; Sensorineural hearing loss

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CONGENITAL MALFORMATION; DENTAL CARE; FEMALE; GOITER; HUMAN; HYPERCEMENTOSIS; LIP; MACROGLOSSIA; MANDIBLE; PERCEPTION DEAFNESS; PERIODONTAL DISEASE; SYNDROME;

ADULT; DENTAL CARE FOR CHRONICALLY ILL; FEMALE; GOITER; HEARING LOSS, SENSORINEURAL; HUMANS; HYPERCEMENTOSIS; LIP; MACROGLOSSIA; MANDIBLE; PERIODONTAL ATTACHMENT LOSS; SYNDROME;

EID: 34249799316     PISSN: 00223492     EISSN: None     Source Type: Journal    
DOI: 10.1902/jop.2007.060270     Document Type: Article

References (41)

1. Pendred V. Deaf mutism and goiter. Lancet 1896; 2:532.
2. Smith RJH, Camp GV. Deafness and hereditary hearing loss overview. Available at: http://www.geneclinics.org/profiles/deafness-overview/ details.html. Accessed May 6, 2006.
3. Fraser GR. Association of congenital deafness with goiter (Pendred's syndrome). Ann Hum Genet 1965; 28:201-249.
4. Coakley JC, Keir EH, Connelly JF. The association of thyroid dyshormonogenesis and deafness (Pendred syndrome): Experience of the Victorian neonatal thyroid screening programme. J Paediatr Child Health 1992;28:398-401.
5. Reardon W, Coffey R, Phelps PD, et al. Pendred syndrome - 100 years of underascertainment? QJM 1997;90:443-447.
6. Sheffield VC, Kraiem Z, Beck JC, Nishimura D, Stone EM, Salameh M. Pendred syndrome maps to chromosome 7q 21-34 and is caused by an intrinsic defect in thyroid iodine organification. Nat Genet 1996;12: 424-426.
7. Gausden E, Coyle B, Armour JAL. Pendred syndrome: Evidence for genetic homogeneity and further refinement of linkage. J Med Genet 1997;34:126-129.
8. Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat Genet 1997;17:411-422.
9. Taylor JP, Metcalfe RA, Watson PF. Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: Implication for thyroid dysfunction in Pendred syndrome. J Clin Endocrinol Metab 2002;87:1778-1784.
10. Glickman I, Smulow JB. Buttressing bone formation in the periodontium. J Periodontol 1965;36:365-370.
11. Kratz A, Sluss PM, Januzzi JL Jr., Lewandrowski KB. Appendices - Laboratory values of clinical importance. In: Kasper DL, Braunwald E, Fauci AS, Hauser SL, Longo DL, Jameson LJ, eds. Harrison's Principles of Internal Medicine, 16th ed. New York: McGraw-Hill; 2005:A1-A15.
12. Serio FG, Hawley CE. Appendix - Reference values for adults. In: Manual of Clinical Periodontics. Hudson, OH: Lexi; 2002:125-127.
13. McCall CE, De Chatelet LR, Butler R, Brown D. Enhanced phagocyte capacity. The biological basis for the elevated histochemical nitroblue tetrazolium reduction. J Clin Invest 1974;54:1227-1234.
14. Izumi Y, Sugiyama S, Shinozuka O, Yamazaki T, Ohyama T, Ishikawa I. Defective neutrophil chemotaxis in Down's syndrome patients and its relationship to periodontal destruction. J Periodontol 1989;60:238-242.
15. Boyden S. The chemotactic effects of mixtures of antibody and antigen on polymorphonuclear leucocytes. J Exp Med 1962; 115:453-456.
16. Giuntoli JM, Estevez ME, Sen L, Penalver J. A defective function of the peripheral blood neutrophils in thalassemia major. Am J Pediatr Hematol Oncol 1984; 6:215-217.
17. Roberts CGP, Ladenson PW. Hypothyroidism. Lancet 2004;363:793-803.
18. 123I for thyroid imaging. J Nucl Med 1976;17:261-267.
19. Gordon B, Yaakob W, Willi S, Buse M, Gordon L. Congenital thyroid disease revisited: Migrational anomalies and dyshormonogenesis. J Nucl Med Technol 1999;27:282-286.
20. Tech KE, Davis L, Dworkin H. Papillary thyroid carcinoma concentrating both Tc-99m sodium pertechnetate and 1-131 iodide. Case report and review of the literature. Clin Nucl Med 1991;16:497-500.
21. Loevy HT, Aduss H, Rosenthal IM. Tooth eruption and craniofacial development in congenital hypothyroidism: Report of case. J Am Dent Assoc 1987; 115:429-431.
22. Weiss LS, White JA. Macroglossia: A review. J La State Med Soc 1990;142:13-16.
23. Soni S, Singh G, Yasir S, Hatipoglu B. An unusual presentation of hypothyroidism. Thyroid 2005;15: 289-291.
24. Kimura S, Yonemura T, Kaya H. Increased oxidative product formation by peripheral blood polymorphonuclear leukocytes in human periodontal diseases. J Periodontal Res 1993;28:197-203.
25. Van Dyke TE, Zinney W, Winkel K, Taufiq A, Offenbacher S, Arnold RR. Neutrophil function in localized juvenile periodontitis-phagocytosis, superoxide production and specific granule release. J Periodontol 1986;57:703-708.
26. Yang YL, Hou LT, Chang WK. Polymorphonuclear neutrophil chemotaxis in Chinese patients with post-juvenile periodontitis and rapidly progressive periodontitis. J Formos Med Assoc 1993;92:643-648.
27. Van Dyke TE, Taubman MA, Ebersole JL, et al. The Papillon-Lefevre syndrome: Neutrophil dysfunction with severe periodontal disease. Clin Immunol Immunopathol 1984;31:419-429.
28. Firatli E, Tüzün B, Efeojlu A. Papillon-Lefeèvre syndrome. Analysis of neutrophil chemotaxis. J Periodontol 1996; 67:617-620.
29. De Toni S, Piva E, Lapolla A, Fontana G, Fedele D, Plebani M. Respiratory burst of neutrophils in diabetic patients with periodontal disease. Ann N Y Acad Sci 1997;832:363-367.
30. Fontana G, Lapolla A, Sanzari M, et al. An immunological evaluation of type II diabetic patients with periodontal disease. J Diabetes Complications 1999; 13:23-30.
31. Suzuki JB, Collison BC, Falkler WA Jr., Nauman RK. Immunologic profile of juvenile periodontitis. II. Neutrophil chemotaxis, phagocytosis and spore germination. J Periodontol 1984;55:461-467.
32. Van Dyke TE, Zinney W, Winkel K, Taufiq A, Offenbacher S, Arnold RR. Neutrophil function in localized juvenile periodontitis - Phagocytosis, superoxide production and specific granule release. J Periodontol 1986;57:703-708.
33. Genco RJ, Van Dyke TE, Levine MJ, Nelson RD, Wilson ME. 1985 Kreshover lecture. Molecular factors influencing neutrophil defects in periodontal disease. J Dent Res 1986;65:1379-1391.
34. Lopez NJ. Clinical, laboratory, and immunological studies of a family with a high prevalence of generalized prepubertal and juvenile periodontitis. J Periodontol 1992;63:457-468.
35. Armitage GC. Development of a classification system for periodontal diseases and conditions. Ann Periodontol 1999;4:1-6.
36. Kinane DF. Periodontitis modified by systemic factors. Ann Periodontol 1999;4:54-64.
37. Lakatos P. Thyroid hormones: Beneficial or deleterious for bone? Calcif Tissue Int 2003;73:205-209.
38. Kisakol G, Kaya A, Gonen S, Tunc R. Bone and calcium metabolism in subclinical autoimmune hyperthyroidism and hypothyroidism. Endocr J 2003; 50:657-661.
39. Souza NL, Lima MS Jr., Pimenta GSFJ, Souza RAAL, Gomez SR. Atypical hypercementosis versus cementoblastoma. Dentomaxillofac Radiol 2004;33: 267-270.
40. Leider AS, Garbarino VE. Generalized hypercementosis. Oral Surg Oral Med Oral Pathol 1987;63: 375-380.
41. Kupfer IJ. Correlation of hypercementosis with toxic goiter. J Dent Res 1951;30:734-736.