Congenital insensitivity to pain - Review and report of a case with dental implications

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics

Volumn 101, Issue 1, 2006, Pages 58-62

  Butler, Jonathan ^a   Fleming, Padraig ^b   Webb, David ^b  

^a TRINITY COLLEGE DUBLIN   (Ireland)

^b OUR LADY S CHILDREN S HOSPITAL   (Ireland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 29144533359     PISSN: 10792104     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tripleo.2005.08.002     Document Type: Article

References (25)

1. G. Dearborn A case of congenital pure analgesia J Nerv Ment Dis 75 1932 612 615
2. S.J. Littlewood, and L. Mitchell The dental problems and management of a patient suffering from congenital insensitivity to pain Int J Paediatr Dent 8 1998 47 50
3. G.A. Nicholson, J.L. Dawkins, I.P. Blair, M.L. Kennerson, M.J. Gordon, and A.K. Cherryson The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3 Nat Genet 13 1996 101 104
4. F.B. Axelrod, and M.J. Hilz Inherited autonomic neuropathies Semin Neurol 23 2003 381 390
5. K. Verhoeven, K. Coen, E. De Vriendt, A. Jacobs, V. Van Gerwen, and I. Smouts SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type 1 Neurology 62 2004 1001 1002
6. R.G. Lafreniere, M.L.E. MacDonald, M.-P. Dube, J. MacFarlane, M. O'Driscoll, and B. Brais Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the study of Canadian genetic isolates Am J Hum Genet 74 2004 1064 1073
7. A. Blumenfeld, S.A. Slaughenhaupt, C.B. Liebert, V. Temper, C. Maayan, and S. Gill Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31 Am J Hum Genet 64 1999 1110 1118
8. S.A. Slaughenhaupt, A. Blumenfeld, S.P. Gill, M. Leyne, J. Mull, and M.P. Cuajungco Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia Am J Hum Genet 68 2001 598 605
9. S. Shatzky, S. Moses, J. Levy, V. Pinsk, E. Hershkovitz, and L. Herzog Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli Bedouins: genetic heterogenicity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies Am J Med Genet 92 2000 353 360
10. E. Einasdottir, A. Carlsson, J. Minde, G. Toolanen, O. Svensson, and G. Solders A mutation in nerve growth factor beta gene (NGFB) causes loss of pain perception Hum Mol Genet 13 2004 799 805
11. E.M. Nagasako, A.L. Oaklander, and R.H. Dworkin Congenital insensitivity to pain: an update Pain 101 2003 213 219
12. P. Rasmussen The congenital insensitivity-to-pain syndrome (analgesia congenita): report of a case Int J Paediatr Dent 6 1996 117 122
13. K.H. Hall Paediatric Orofacial Medicine and Pathology 1994 Chapman & Hall Medical London p. 330-5
14. V. Narayanan Oral and maxillofacial manifestations of hereditary sensory neuropathy Br J Oral Maxillofac Surg 34 1996 446 449
15. F.B. Axelrod, and J. Pearson Congenital sensory neuropathies: diagnostic distinction from familial dysautonomia Am J Dis Child 138 10 1984 947 954
16. C.C. Thompson, R.I. Park, and G.H. Prescott Oral manifestations of the congenital insensitivity to pain syndrome Oral Surg Oral Med Oral Pathol Oral Radiol Endod 50 1980 220 225
17. A. Amano, S. Akiyama, M. Ikeda, and I. Morisaki Oral manifestations of hereditary sensory and autonomic neuropathy type IV. Congenital insensitivity to pain with anhidrosis Oral Surg Oral Med Oral Pathol Oral Radiol Endod 86 1998 425 431
18. M. Diab Self-inflicted orodental injury in a child with Leigh disease Int J Paediatr Dent 14 2004 73 77
19. R.J. Gorlin, M.M. Cohen Jr., and L.S. Levin Syndromes of the Head and Neck 3rd ed. 1990 Oxford University Press New York p. 598-601
20. J. Pedersen, K. Stensgaard, and B. Melsen Prevalence of malocclusion in relation to premature loss of primary teeth Community Dent Oral Epidemiol 6 1978 204 209
21. J.G. Dale T.M. Graber R.L. Vanardsall Orthodontics - current principles and techniques 1994 Mosby-Year Book 315 317
22. T.L. Erdem, I. Ozcan, D. Ilguy, and S. Sirin Hereditary sensory and autonomic neuropathy: review and a case report with dental implications J Oral Rehabil 27 2000 180 183
23. M. Auer-Grumbach Hereditary sensory neuropathies Drugs Today (Barc) 40 2004 385 394
24. C.M. Eng, S.A. Slaughenhaupt, A. Blumenfeld, F.B. Axelrod, J.F. Gusela, and R.J. Desnick Prenatal diagnosis of familial dysautonomia by analysis of linked CA-repeat polymorphisms on chromosome 9q31-q33 Am J Med Genet 59 1995 349 355
25. C. Oddoux, E. Reich, F. Axelrod, A. Blumenfeld, C. Maayan, and S. Slaughenhaupt Prenatal diagnostic testing for familial dysautonomia using linked genetic markers Prenat Diagn 15 1995 817 826