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2009 | OriginalPaper | Hoofdstuk

10. Tandheelkundige afwijkingen bij het ehlers-danlos syndroom

Auteur : P.J. De Coster

Gepubliceerd in: Het tandheelkundig jaar 2009

Uitgeverij: Bohn Stafleu van Loghum

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Samenvatting

Het ehlers-danlos syndroom (EDS) groepeert een aantal erfelijke aandoeningen van het bindweefsel die hypermobiele gewrichten, hyperelasticiteit van de huid en een ernstig verhoogde weefselkwetsbaarheid als gemeenschappelijke symptomen hebben. Tegenwoordig worden wereldwijd twee verwante classificatiesystemen gehanteerd die werden opgesteld door een multidisciplinair team van genetici, pediaters en endocrinologen. Een eerste formele classificatie (Berlin Nosology) werd opgesteld in 1986 (Beighton et al., 1988) en onderscheidde tien EDS-typen op basis van klinische symptomen en erfelijke overdracht. Het ontrafelen van de moleculaire mechanismen achter deze aandoeningen genereerde echter vrij snel de behoefte aan het opstellen van een vereenvoudigde classificatie met een duidelijke afbakening van de diagnostische parameters.
Literatuur
go back to reference LiteratuurArendt-Nielsen L, Kaalund S, Bjerring P, H0gsaa B. Insufficient effect of local analgesics in Ehlers danlos type III patients (connective tissue disorder). Acta Anaesthesiol Scand. 1990;34:358–61.CrossRef LiteratuurArendt-Nielsen L, Kaalund S, Bjerring P, H0gsaa B. Insufficient effect of local analgesics in Ehlers danlos type III patients (connective tissue disorder). Acta Anaesthesiol Scand. 1990;34:358–61.CrossRef
go back to reference Barabas GM, Barabas AP.The Ehlers-danlos syndrome. A report of the oral and haematological findings in nine cases. Br Dent J. 1967;123:473–9.PubMed Barabas GM, Barabas AP.The Ehlers-danlos syndrome. A report of the oral and haematological findings in nine cases. Br Dent J. 1967;123:473–9.PubMed
go back to reference Beighton P, Paepe A de, Danks D, Finidori G, Gedde-Dahl T, Goodman R, Hall JG, Hollister DW, Horton W, McKusick VA. International nosology of heritable disorders of connective tissue, Berlin, 1986. Am J Med Genet. 1988;29:581–94.PubMedCrossRef Beighton P, Paepe A de, Danks D, Finidori G, Gedde-Dahl T, Goodman R, Hall JG, Hollister DW, Horton W, McKusick VA. International nosology of heritable disorders of connective tissue, Berlin, 1986. Am J Med Genet. 1988;29:581–94.PubMedCrossRef
go back to reference Beighton P, Paepe A de, Steinmann B, Tsipouras P, Wenstrup RJ. Ehlers-danlos syndromes: Revised nosology, Villefranche, 1997. Am J Med Genet. 1998;77:31–7.PubMedCrossRef Beighton P, Paepe A de, Steinmann B, Tsipouras P, Wenstrup RJ. Ehlers-danlos syndromes: Revised nosology, Villefranche, 1997. Am J Med Genet. 1998;77:31–7.PubMedCrossRef
go back to reference Beighton P. Hypermobility scoring. Br J Rheumatol. 1988;27:163. Beighton P. Hypermobility scoring. Br J Rheumatol. 1988;27:163.
go back to reference Biesecker LG, Erickson RP, Glover TW, Bonadio J. Molecular and cytologic studies of Ehlers- danlos syndrome type VIII. Am J Med Genet. 1991;41:284–8. Biesecker LG, Erickson RP, Glover TW, Bonadio J. Molecular and cytologic studies of Ehlers- danlos syndrome type VIII. Am J Med Genet. 1991;41:284–8.
go back to reference Coster PJ de, Berghe LI van den, Martens LC. Generalized joint hypermobility and temporomandibular disorders: inherited connective tissue disease as a model with maximum expression. J Orofac Pain. 2005b;19:47–57. Coster PJ de, Berghe LI van den, Martens LC. Generalized joint hypermobility and temporomandibular disorders: inherited connective tissue disease as a model with maximum expression. J Orofac Pain. 2005b;19:47–57.
go back to reference Coster PJ de, Cornelissen M, Paepe A de, Martens LC, Vral A. Abnormal dentin structure in two novel gene mutations (COL1A1, Arg134Cys) and (ADAMTS2, Trp795-to-ter) causing rare type I collagen disorders. Arch Oral Biol. 2007;52:101–9.PubMedCrossRef Coster PJ de, Cornelissen M, Paepe A de, Martens LC, Vral A. Abnormal dentin structure in two novel gene mutations (COL1A1, Arg134Cys) and (ADAMTS2, Trp795-to-ter) causing rare type I collagen disorders. Arch Oral Biol. 2007;52:101–9.PubMedCrossRef
go back to reference Coster PJ de, Malfait F, Martens LC, Paepe A de. Unusual oral findings in dermatosparaxis (Ehlers-danlos syndrome type VIIC). J Oral Pathol Med. 2003;32:568–70.PubMedCrossRef Coster PJ de, Malfait F, Martens LC, Paepe A de. Unusual oral findings in dermatosparaxis (Ehlers-danlos syndrome type VIIC). J Oral Pathol Med. 2003;32:568–70.PubMedCrossRef
go back to reference Coster PJ de, Martens LC, Berghe L van den. Prevalence of temporomandibular joint dysfunction in Ehlers-danlos syndromes. Orthod Craniofac Res. 2004b;7:237–240. Coster PJ de, Martens LC, Berghe L van den. Prevalence of temporomandibular joint dysfunction in Ehlers-danlos syndromes. Orthod Craniofac Res. 2004b;7:237–240.
go back to reference Coster PJ de, Martens LC, Paepe A de. Oral health in prevalent types of Ehlers-danlos syndromes. J Oral Pathol Med. 2005a;34:298–307.PubMedCrossRef Coster PJ de, Martens LC, Paepe A de. Oral health in prevalent types of Ehlers-danlos syndromes. J Oral Pathol Med. 2005a;34:298–307.PubMedCrossRef
go back to reference Coster PJ de. Harde tandweefsels en bindweefselstoornissen. In: Het Tandheelkundig Jaar 2004 (pp. 169-184). Houten/Diegem: Bohn Stafleu van Loghum, 2005. Coster PJ de. Harde tandweefsels en bindweefselstoornissen. In: Het Tandheelkundig Jaar 2004 (pp. 169-184). Houten/Diegem: Bohn Stafleu van Loghum, 2005.
go back to reference Elsas LJ 2nd, Miller RL, Pinnell SR. Inherited human collagen lysyl hydroxylase deficiency: ascorbic acid response. J Pediatr. 1978;92:378–84.PubMedCrossRef Elsas LJ 2nd, Miller RL, Pinnell SR. Inherited human collagen lysyl hydroxylase deficiency: ascorbic acid response. J Pediatr. 1978;92:378–84.PubMedCrossRef
go back to reference Felice C de, Biancardi G, Dileo L, Latini G, Parrini S. Abnormal oral vascularnetwork geomteric complexity in Ehlers-danlos syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004;98:429–34.PubMedCrossRef Felice C de, Biancardi G, Dileo L, Latini G, Parrini S. Abnormal oral vascularnetwork geomteric complexity in Ehlers-danlos syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004;98:429–34.PubMedCrossRef
go back to reference Felice C de, Toti P, Di Maggio G, Parrini S, Bagnoli F. Absence of the inferior labial and lingual frenula in Ehlers-danlos syndrome. Lancet. 2001;357:1500–2.PubMedCrossRef Felice C de, Toti P, Di Maggio G, Parrini S, Bagnoli F. Absence of the inferior labial and lingual frenula in Ehlers-danlos syndrome. Lancet. 2001;357:1500–2.PubMedCrossRef
go back to reference Fridrich KL, Fridrich HH, Kempf KK, Moline DO. Dental implications in Ehlers-danlos syndrome. A case report. Oral Surg Oral Med Oral Pathol. 1990;69:431–5.PubMedCrossRef Fridrich KL, Fridrich HH, Kempf KK, Moline DO. Dental implications in Ehlers-danlos syndrome. A case report. Oral Surg Oral Med Oral Pathol. 1990;69:431–5.PubMedCrossRef
go back to reference Gorlin RJ, Cohen MM, Levin LS. Ehlers-danlos syndromes. In Syndromes of the head and neck, 3rd Ed. (pp. 429-41). New York: Oxford University Press, 1990. Gorlin RJ, Cohen MM, Levin LS. Ehlers-danlos syndromes. In Syndromes of the head and neck, 3rd Ed. (pp. 429-41). New York: Oxford University Press, 1990.
go back to reference Hagberg C, Berglund B, Korpe L, Andersson-Norinder J. Ehlers-danlos Syndrome (EDS) focusing on oral symptoms: a questionnaire study. Orthod Craniofac Res. 2004;7:178–85.PubMedCrossRef Hagberg C, Berglund B, Korpe L, Andersson-Norinder J. Ehlers-danlos Syndrome (EDS) focusing on oral symptoms: a questionnaire study. Orthod Craniofac Res. 2004;7:178–85.PubMedCrossRef
go back to reference Hartsfield JK Jr, Kousseff BG. Phenotypic overlap of Ehlers-danlos syndrome types IV and VIII. Am J Med Genet. 1990;37:465–70.PubMedCrossRef Hartsfield JK Jr, Kousseff BG. Phenotypic overlap of Ehlers-danlos syndrome types IV and VIII. Am J Med Genet. 1990;37:465–70.PubMedCrossRef
go back to reference Hoff M. Dental manifestations in Ehlers-danlos syndrome. Report of a case. Oral Surg Oral Med Oral Pathol. 1977;44:864–71.CrossRef Hoff M. Dental manifestations in Ehlers-danlos syndrome. Report of a case. Oral Surg Oral Med Oral Pathol. 1977;44:864–71.CrossRef
go back to reference Létourneau Y, Pérusse R, Buithieu H. Oral manifestations of Ehlers-danlos syndrome. J Can Dent Assoc. 2001;67:330–4.PubMed Létourneau Y, Pérusse R, Buithieu H. Oral manifestations of Ehlers-danlos syndrome. J Can Dent Assoc. 2001;67:330–4.PubMed
go back to reference Linch DC, Acton CH. Ehlers-danlos syndrome presenting with juvenile destructive periodontitis. Br Dent J. 1979;147:95–6.PubMedCrossRef Linch DC, Acton CH. Ehlers-danlos syndrome presenting with juvenile destructive periodontitis. Br Dent J. 1979;147:95–6.PubMedCrossRef
go back to reference Malfait F, Coster PJ de, Hausser I, Essen AJ van, Franck P, Colige A, Nusgens B, Martens L, De Paepe A. The natural history, including orofacial features of three patients with Ehlers-danlos syndrome, dermatosparaxis type (EDS type VIIC). Am J Med Genet. 2004;131:18–28.PubMedCrossRef Malfait F, Coster PJ de, Hausser I, Essen AJ van, Franck P, Colige A, Nusgens B, Martens L, De Paepe A. The natural history, including orofacial features of three patients with Ehlers-danlos syndrome, dermatosparaxis type (EDS type VIIC). Am J Med Genet. 2004;131:18–28.PubMedCrossRef
go back to reference Melamed Y, Barkai G, Frydman M. Multiple supernumerary teeth (MSNT) and Ehlers- danlos syndrome (EDS): a case report. J Oral Pathol Med. 1994;23:88–91.PubMedCrossRef Melamed Y, Barkai G, Frydman M. Multiple supernumerary teeth (MSNT) and Ehlers- danlos syndrome (EDS): a case report. J Oral Pathol Med. 1994;23:88–91.PubMedCrossRef
go back to reference Norton LA, Assael LA. Orthodontic and temporomandibular joint considerations in treatment of patients with Ehlers-danlos syndrome. Am J Orthod Dentofacial Orthop. 1997;111:75–84. Norton LA, Assael LA. Orthodontic and temporomandibular joint considerations in treatment of patients with Ehlers-danlos syndrome. Am J Orthod Dentofacial Orthop. 1997;111:75–84.
go back to reference Ooshima T, Abe K, Kohno H, Izumitani A, Sobue S. Oral manifestations of Ehlers-danlos syndrome type VII: histological examination of a primary tooth. Pediatr Dent. 1990;12:102–6.PubMed Ooshima T, Abe K, Kohno H, Izumitani A, Sobue S. Oral manifestations of Ehlers-danlos syndrome type VII: histological examination of a primary tooth. Pediatr Dent. 1990;12:102–6.PubMed
go back to reference Paepe A de, Malfait F. Bleeding and bruising in patients with Ehlers-danlos syndrome and other collagen vascular disorders. Br J Haematol. 2004;127:491–500.CrossRef Paepe A de, Malfait F. Bleeding and bruising in patients with Ehlers-danlos syndrome and other collagen vascular disorders. Br J Haematol. 2004;127:491–500.CrossRef
go back to reference Reichert S, Riemann D, Plaschka B, Machulla HK. Early-onset periodontitis in a patient with Ehlers-danlos syndrome type III. Quintessence Int.1999;30:785–90.PubMed Reichert S, Riemann D, Plaschka B, Machulla HK. Early-onset periodontitis in a patient with Ehlers-danlos syndrome type III. Quintessence Int.1999;30:785–90.PubMed
go back to reference Sadeghi EM, Ostertag PR, Eslami A. Oral manifestations of Ehlers-danlos syndrome: report of case. J Am Dent Assoc. 1989;118:189–91.CrossRef Sadeghi EM, Ostertag PR, Eslami A. Oral manifestations of Ehlers-danlos syndrome: report of case. J Am Dent Assoc. 1989;118:189–91.CrossRef
go back to reference Slootweg PJ, Beemer FA. Gingival fibrinoid deposits in Ehlers-danlos syndrome. J Oral Pathol. 1987;16:150–2.PubMedCrossRef Slootweg PJ, Beemer FA. Gingival fibrinoid deposits in Ehlers-danlos syndrome. J Oral Pathol. 1987;16:150–2.PubMedCrossRef
go back to reference Stewart RE, Hollister DW, Rimoin DL. A new variant of Ehlers-danlos syndrome: an autosomal dominant disorder of fragile skin, abnormal scarring, and generalized periodontitis. Defects Orig Artic Ser. 1977;13:85–93. Stewart RE, Hollister DW, Rimoin DL. A new variant of Ehlers-danlos syndrome: an autosomal dominant disorder of fragile skin, abnormal scarring, and generalized periodontitis. Defects Orig Artic Ser. 1977;13:85–93.
go back to reference Stine KC, Becton DL. DDAVP therapy controls bleeding in Ehlers-danlos syndrome. J Pediatr Hematol Oncol. 1997;19:15 Stine KC, Becton DL. DDAVP therapy controls bleeding in Ehlers-danlos syndrome. J Pediatr Hematol Oncol. 1997;19:15
Metagegevens
Titel
Tandheelkundige afwijkingen bij het ehlers-danlos syndroom
Auteur
P.J. De Coster
Copyright
2009
Uitgeverij
Bohn Stafleu van Loghum
DOI
https://doi.org/10.1007/978-90-313-6612-5_10