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Craniofacial and Dental Characteristics of Kabuki Syndrome: Nine Years Cephalometric Follow-Up

  • Tuna EB1,*,
  • Marşan G1
  • Gençay K1
  • Seymen F1

1Istanbul University Faculty of Dentistry, Department of Pedodontics, Capa, 34093 Istanbul, Turkey.

DOI: 10.17796/jcpd.36.4.u021164272805116 Vol.36,Issue 4,July 2012 pp.393-400

Published: 01 July 2012

*Corresponding Author(s): Tuna EB E-mail: ebtuna@istanbul.edu.tr

Abstract

Kabuki syndrome is a rare autosomal dominant trait with variable clinical expression. Common dental manifestations of Kabuki syndrome are high-arched palate, micrognathia, malocclusion, microdontia, small dental arches, hypodontia, severe maxillary recession and mid-facial hypoplasia. Study design: This report includes the oral manifestations of a Turkish patient with Kabuki syndrome with consideration of the long-term craniofacial prognosis for this patient based on the physical, clinical and radiological findings in 9 years follow-up period. General appearance of the patient was characterized by postnatal growth retardation, moderate mental retardation, peculiar face characterized by long palpebral fissures with eversion of the lateral third of the lower eyelids, prominent and cup-shaped ears, broad and depressed nasal tips, short fifth fingers, psychomotor retardation and dermatologic abnormalities. Results and conclusion: Cephalometric analysis revealed skeletal open bite; periapical and panoramic radiographic examinations showed agenesis permanent teeth. A patient with Kabuki syndrome, who may lead to a better understanding of the abnormalities, playing an important role in clinical diagnosis, planning and dental management is presented.

Keywords

craniofacial growth, Kabuki syndrome, dental characteristics, cephalometric analysis.

Cite and Share

Tuna EB,Marşan G,Gençay K,Seymen F. Craniofacial and Dental Characteristics of Kabuki Syndrome: Nine Years Cephalometric Follow-Up. Journal of Clinical Pediatric Dentistry. 2012. 36(4);393-400.

References

1. Adam MP, Hudgins L. Kabuki syndrome: a review. Clin Genet, 67: 209–219, 2005.

2. Matsumoto N, Niikawa N. Kabuki make-up syndrome: a review. Am J Med Genet Part C, 117: 57–65, 2003.

3. Niikawa N, Matsuura N, Fukushima Y, Ohsawa T, Kayii T. Kabuki make-up syndrome: a syndrome of mental retardation, unusual facies, large and protruding ears, and postnatal growth deficiency. J Pediatr, 99: 565–569, 1981.

4. Kuroki Y, Suzuki Y, Chyo H, Hata A, Matsui I. A new malformation syndrome of long palpebral fissures, large ears, depressed nasal tip, and skeletal anomalies associated with postnatal dwarfism and mental retardation. J Pediatr, 99: 570–573, 1981.

5. Ng SB, Bigham AW, Buckingham KJ, Hannibal MC, McMillin MJ, Gildersleeve HI, Beck AE, Tabor HK, Cooper GM, Mefford HC, Lee C, Turner EH, Smith JD, Rieder MJ, Yoshiura K, Matsumoto N, Ohta T, Niikawa N, Nickerson DA, Bamshad MJ, Shendure J. Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome. Nat Genet, 42: 790–793, 2010.

6. Armstrong L, Abd El Moneim A, Aleck K, Aughton DJ, Baumann C, Braddock SR, Gillesen-Kaesbach G, Graham JMJ, Grebe TA, Grip KW, Hall BD, Hennekom R, Hunter A, Kepler-Noreuil K, Lacombe D, Lin AE, Ming JE, Kokitsu-Nakata NM, Nikel SM, Phillip N, RassRothschild A, Sommer A, Verloes A, Walter C, Wieczorek D, Williams MS, Zackai E, Allanson JE. Further delineation of Kabuki syndrome in 48 well-defined new individuals. Am J Med Genet, 132A: 265–72, 2005.

7. Atar M, Lee W, O’Donnell D. Kabuki syndrome: oral and general features seen in a 2-year-old Chinese boy. Int J Paediatr Dent, 16: 222–226, 2006.

8. Kobayashi E, Maruyama Y, Kobayashi K. A longitudinal evaluation of craniofacial growth in a patient with Kabuki make-up syndrome: a case report. Eur J Orthod, 23: 205–213, 2001.

9. Matsune K, Shimizu T, Tohma T, Asada Y, Ohashi H, Maeda T. Craniofacial and dental characteristics of Kabuki syndrome. Am J Med Genet, 98: 185–190, 2001.

10. Takada K, Fukushima H, Watanabe S, Ishida M, Ogasawara H, Motokawa W. Occlusal guidance of two Kabuki make-up syndrome patients: case reports. J Clin Pediatr Dent, 28: 113–118, 2004.

11. Lerone M, Priola M, Naselli A, Vignolo M, Romeo G, Silengo MC. Ectodermal abnormalities in Kabuki syndrome. Am J Med Genet, 73: 263–266, 1997.

12. dos Santos BM, Riberio RR, Stuani AS, de Paula e Silva FW, de Queiroz AM. Kabuki make-up (Niikawa-Kuroki) syndrome: dental and craniofacial findings in a Brazilian child. Braz Dent J, 17: 249–254, 2006.

13. Gidwani P, Segal E, Shanske A, Driscoll C. Chorea associated with antiphospholipid antibodies in a patient with Kabuki syndrome. Am J Med Genet, 143A: 1338–1341, 2007.

14. Jacobson A. Radiographic cephalometry from basics to video-imaging 1995, Quintessence Publishing Co. Inc.: 242–244, 1995.

15. Niikawa N, Kuroki Y, Kajii T, Matsuura N, Ishikiriyama S, Tonoki H, Ishikawa N, Yamada Y, Fujita M, Umemoto H, Iwama Y, Kondoh I, Fukushima Y, Nako Y, Matsui I, Urakami T, Aritaki S, Hava M, Suzuki Y, Chyo H, Sugio Y, Hasegawa T, Yamanaka T, Tsukino R, Yoshida A, Nomoto N, Kawahito S, Aihara R, Toyota S, Leshima A, Funaki H, Ishitobi K, Ogura S, Furumae T, Yoshino M, Tsuji Y, Kondoh T, Matsomoto T, Abe K, Harada N, Miike T, Ohda S, Naritomi K, Abushwereb AK, Braun OH, Schmid E. Kabuki make-up (NiikawaKuroki) syndrome: a study of 62 patients. Am J Med Genet, 31: 565–589, 1988.

16. Burke LW, Jones MC. Kabuki syndrome: underdiagnosed recognizable pattern in cleft palate patients. Cleft Palate Craniofac J, 32: 77–84, 1995.

17. Gillis R, Klar A, Gross-Kieselstein A. The Niikawa-Kuroki (Kabuki make-up syndrome in a Moslem Arab child. Clin Genet, 38: 378–381, 1990.

18. Galan-Gomez E, Cardesa-Garcia JJ, Campo-Sampedro FM, Salamanca-Maesso C, Martinez-Frias ML, Frias JL. Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children. Am J Med Genet, 59: 276–282, 1995.

19. Lung ZH, Rennie A. Kabuki syndrome: a case report. J Orthod, 33: 242–245, 2006.

20. Franceschini P, Vardeu MP, Guala A, Franceschini D, Testa A, Corrias A, Chiabotto P. Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa–Kuroki) syndrome. Am J Med Genet, 47: 423–425, 1993.

21. Ioan DM, Fryns JP. Kabuki syndrome: description of a 2-year old Roumanian boy and review of the literature. Genet Couns, 18: 113–117, 2007.

22. Maas N M C, Van de Putte T, Melotte C, Francis A, Schrander-Stumpel CTRM, Sanlaville D, Genevieve D, Lyonnet S, Dimitrov B, Devriendt K, Fryns J P, Vermeesch JR. The C20orf133 gene is disrupted in a patient with Kabuki syndrome. J Med Genet, 44: 562–569, 2007.

23. Genevieve D, Amiel J, Viot G, Le Merrer M, Sanlaville D, Urtizberea A, Gerard M, Munnich A, Cormier-Daire V, Lyonnet S. A typical findings in Kabuki syndrome: report of 8 patients in a series of 20 and review of the literature. Am J Med Genet, 129: 64–68, 2004.

24. White SM, Thompson EM, Kidd A, Savarirayan R, Turner A, Amor D, Delatycki MB, Fahey M, Baxendale A, White S, Haan E, Gibson K, Halliday JL, Bankier A. Growth, behaviour and clinical findings in 27 patients with Kabuki (Niikawa-Kuroki) syndrome. Am J Med Genet, 127A: 118–127, 2004.

25. Halal F, Gledhill R, Dudkiewicz A. Autosomal dominant inheritance of the Kabuki make-up (Niikawa-Kuroki) syndrome. Am J Med Genet, 33: 376–381, 1989.

26. Kobayashi O, Sakuragawa N. Inheritance in Kabuki make-up (Niikawa-Kuroki) syndrome. (Letter) Am J Med Genet, 61: 92–93, 1996.

27. Silengo M, Lerone M, Seri M, Romeo G. Inheritance of NiikawaKuroki (Kabuki make-up) syndrome. Am J Med Genet, 66: 368, 1996.

28. Tsukahara M, Kuroki Y, Imaizumi K, Miyazawa Y, Matsuo K. Dominant inheritance of Kabuki make-up syndrome. Am J Med Genet, 73: 19–23, 1997.

29. Courtens W, Rassart A, Stene JJ, Vamos E. Further evidence for autosomal dominant inheritance and ectodermal abnormalities Kabuki syndrome. Am J Med Genet, 93: 244–249, 2009.

30. Li M, Zackai E H, Niikawa N, Kaplan P, Driscoll DA. Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocadiofacial chromosomal region within 22q 11.2. Am J Med Genet, 65: 101–103, 1996.

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