Case Report Endodontic management of a hypertaurodontic tooth associated with 48, XXYY syndrome: A review and case report Sridevi Krishnamoorthy#, Velayutham Gopikrishna* Department of Conservative Dentistry and Endodontics, Thai Moogambigai Dental College, Dr. MGR Educational and Research Institute University, Chennai, Tamil Nadu, India

Abstract is a developmental anomaly of a tooth characterized by large pulp chamber and short roots. Patients with multiple taurodontic teeth are associated with the probability of a systemic syndrome or chromosomal anomaly. This is the first reported incidence of the endodontic management of a hyper taurodontic mandibular second molar in a patient diagnosed with 48, XXYY syndrome. Keywords: XXY/; 48, XXYY syndrome; hypertaurodontism

INTRODUCTION Multiple taurodontic teeth may occur as one of the dental manifestations of XXYY syndrome. The presence of XXYY syndrome also known as 48, XXYY syndrome or “double taurodontic teeth can facilitate early recognition of this male syndrome” is a rare sex chromosome disorder. This could provide means for an effective systemic condition characterized by presence of two extra X and Y rehabilitation.[4] This is the first reported incidence of the chromosomes with an incidence of 1:18,000-1:40,000 male endodontic management of a hypertaurodontic mandibular births.[1-3] This syndrome is clinically manifested later in life molar tooth in a patient diagnosed with 48, XXYY syndrome. with developmental delays, learning disabilities, behavioral problems, and delayed or incomplete puberty. Many cases go CASE REPORT undiagnosed as most of the above mentioned abnormalities [4,5] do not develop until early puberty. A 19-year-old male reported to the postgraduate department of endodontics of our dental school, for The term taurodontism was coined by Sir Arthur Kein management of multiple carious teeth. During history [6] to describe the bull-like appearance of the teeth. taking, it was elicited that the patient was a school dropout Taurodontism can be defined as a morphological variation due to difficulty in coping with the educational curriculum. of a tooth in which the pulp chamber is vertically elongated It was also evident, that the patient had below average and the roots are reduced in size. Taurodontic teeth have communication skills with low self-esteem. The patient’s large pulp chambers with apically positioned furcation medical history was noncontributory. The patient’s dental area.[7] The etiology of taurodontism is attributed to the history revealed episodes of recurrent caries and multiple failure of Hertwig epithelial root sheath diaphragm to extractions. Extraoral examination revealed retruded mid invaginate at the proper horizontal level.[6] Based on the face with mandibular prognathism [Figure 1]. severity, taurodontic teeth can be classified ashypo-, meso- , and hypertaurodont forms. Hypotaurodont expresses the Intraoral examination revealed dental caries in relation to least pronounced changes, while mesotaurodont expresses moderate variation, and hypertaurodont is characterized teeth 15, 37, and 47 and multiple missing teeth (14, 13, by the most severe variation in which the roots bifurcate or 22, 23, and 36). An orthopantomograph revealed multiple trifurcate close to the apices.[8] taurodontic teeth in relation to 37, 46, 47, 17, 26, and 27 [Figure 2a]. The taurodontic teeth exhibited large pulp Address for correspondence: Dr. Velayutham Gopikrishna, Department of Conservative Access this article online Dentistry and Endodontics, Thai Moogambigai Dental College, Quick Response Code: Dr. MGR Educational and Research Institute University, Golden Website: George Nagar, Chennai - 600 107, Tamil Nadu, India. www.jcd.org.in E-mail: [email protected] Date of submission : 02.01.2015 DOI: Review completed : 10.03.2015 10.4103/0972-0707.157269 Date of acceptance : 17.03.2015

Journal of Conservative Dentistry | May-Jun 2015 | Vol 18 | Issue 3 265 Krishnamoorthy and Gopikrishna: Endodontic management of a hypertaurodontic tooth associated with 48, chamber extending beyond the cervical area and reaching of 17% ethylenediaminetetraacetic acid (EDTA; Smearclear, the furcation suggestive of hypertaurodontism. On clinical SybronEndo, CA, USA). Final irrigation was done using examination, tooth 37 showed no response to electric 5.2%NaOCl. The canals were dried using sterile paper points and cold test. The tooth was nonsensitive to percussion, and dressed with intracanal calcium hydroxide medicament and radiographic interpretation was suggestive of and the tooth was sealed temporarily with an intermediate asymptomatic apical periodontitis. A decision was made restorative material (CavitG, 3M-ESPE, Seefeld, Germany). to perform orthograde root canal treatment in 37. The patient was informed about the complex root anatomy and The patient was asked to return after 2 weeks. At the possible complications. Patient consent was obtained prior second appointment, copious irrigation was done in order to commencement of treatment. to remove the calcium hydroxide and the canals were made dry with sterile paper points. Following radiographic The complete endodontic management of the case was control of the fit of gutta-percha mastercone (Guttapercha, performed by one of the author,# while the other author* SybronEndo, CA, USA), the apical part of the main root took care of post-endodontic restoration and clinical canals was obturated with vertically compacted warm follow-up with department of oral surgery. The patient was gutta-percha using the Touch&Heat 5004 device (Sybron anesthetized with 1.7 ml of 4% articaine with 1:100,000 Endo, CA, USA). The coronal portion of the main canal was epinephrine (Septocaine, Septodont, New Castle, DE, USA) backfilled with thermoplasticized gutta-percha using the and access opening was performed under rubber dam Obtura IIgun (Obtura-Spartan Corp, Fenton, MO, USA). The isolation. Endodontic treatment in taurodontic teeth has access cavity was sealed with dualcuredcomposite resin been described as difficult as the complex morphology (ParaCore, Coltene/Whaledent, NJ, USA). A full coverage could hamper the location of the root canal orifices. The crown was restored on the tooth after 3 weeks’ time. access opening and canal tracing was performed with The patient was then referred to the Department of Oral the help of adental operating microscope (G6, Global Surgery for surgical correction of prognathic mandible. Microscope, USA). Careful inspection and exploration The surgical intervention was performed in two stages. revealed a large coronal pulp chamber extending 8-10 mm The first stage involved a bilateral sagittal split osteotomy below the cervical margin (cementoenamel junction (CEJ)). followed after 3 months by a second stage surgical The presence of two canals (mesial and distal) bifurcating advancement genioplasty procedure. Follow-up was at 3-4 mm short of the radiographic apex was identified. An 6-months and 2-year intervals [ ure 1b and c]. Patient electronic apex locator (Root ZX, Morita, Tokyo Japan) was remained asymptomatic at these times. used to determine the working length. The shaping and cleaning of all canals was done using nickel-titanium rotary DISCUSSION instruments, K3 (Sybron Endo, Orange, CA, USA). Irrigation was done with 5.2% sodium hypochlorite solution (NaOCl) A normal individual has 22 pairs of (numbered during shaping and cleaning of the root canal system. chromosomes) and one pair of autosomes and a single X and Passive ultrasonic irrigation (PUI) activation was employed , making a or chromosomal makeup using # 20/0.00 taper SS noncutting ultrasonic tip (Irrisafe, of 46, XY. Similarly, a normal female has 22 pairs of autosomes Satelec, Acteon, Merignae, France) followed by 1 min flush and two X chromosomes, making a karyotype 46, XX.

a b a

c b c Figure 1: (a) Preoperative extraoral photograph showing Figure 2: (a) Preoperative orthopantomograph before the mandibular prognathism. (b and c) Postsurgical photograph rootcanal treatment. (b) Immediate postoperative radiograph. after bilateral sagittal split osteotomy and genioplasty (c) A 2-year follow-up post endodontic restoration in 37

266 Journal of Conservative Dentistry | May-Jun 2015 | Vol 18 | Issue 3 Krishnamoorthy and Gopikrishna: Endodontic management of a hypertaurodontic tooth associated with 48, xxyy syndrome

48, XXYY syndrome is characterized by an extra as an isolated manifestation or in association with various and an extra Y chromosome. This, in addition to the 22 pairs systemic syndromes. A literature search for relevant of autosomes, males with 48, XXYY syndrome has four sex articles regarding endodontic management of taurodontic chromosomes, making a karyotype 48, XXYY. Successive tooth associated with systemic syndromes was performed meiotic nondisjuctional events during , using Ovid MEDLINE®, Cochrane Database of Systemic resulting in a XYY sperm have been attributed as the most Reviews, Embase, and PubMed. Table 1 summarizes the probable etiological mechanism of 48, XXYY syndrome. The chronological order of case reports of taurodontism presence of extra sex chromosomes may lead to altered associated with systemic syndromes. deoxyribonucleic acid (DNA) methylation at various loci in genome leading to altered gene expression and subsequent phenotype variation.[2,3]

According to Gardner and Girgis,[9] a patient with multiple taurodontic teeth without known association of any systemic syndrome should be consulted for chromosomal analysis, as there is a higher association of taurodontic teeth with X-chromosome aneuploidy syndromes. Hence, we referred our patient to the department of human genetics for chromosomal analysis. Chromosome analysis with GTG banding with a resolution of 450-550 bp, showed a numerical abnormality in all cells analyzed, with the presence of an extra X and an extra Y chromosome resulting in 48 chromosomes and a diagnosis of 48, XXYY syndrome was made [Figure 3]. Figure 3: Chromosome analysis with GTG banding showing The prevalence of taurodontism ranges from 2.5 to 11.3% numerical abnormality in all cells with presence of extra X of the human population.[10] Taurodontism can occur either and Y chromosome

Table 1: Chronological reports of systemic syndromes associated with taurodontism Year Syndrome Author Chromosomal disorder 1970 Mohr syndrome Gorlin[11] Autosomal recessive 1973 Klienfelter syndrome Mednick[12] Additional X chromosome 1978 Tricho-onycho-dental syndrome Koshiba et al.[13] Autosomal dominant 1981 Downs syndrome Jaspers[14] Additional 21 chromosome 1991 Prader-Labhart-Willi syndrome Bassarelli et al.[15] Gene at 1997 Lowe syndrome Tsai and O’Donnell[16] X-linked recessive 1998 Tricho-dento-osseous syndrome Spangler et al.[17] Autosomal dominant 1998 Wolf-Hirschhorn syndrome Breen[18] Partial deletion of the terminal portion of the short arm of 1998 Ellis-van Creveld syndrome Hunter and Roberts[19] Autosomal dominant 2001 Apert syndrome Terezhalmy et al.[20] Autosomal dominant 2002 Seckel syndrome Seymen et al.[21] Autosomal recessive 2003 McCune-Albright syndrome Akintoye et al.[22] Autosomal dominant 2003 Lenz microphthalmia syndrome Ersin et al.[23] X-linked recessive 2003 Kabuki syndrome Petzold et al.[24] Autosomal dominant 2005 Axelsson[25] Gene deletion at 2006 Smith-Magenis syndrome Tomona et al.[26] Gene deletion at chromosome 7 2015 XXYY syndrome Our present case report Additional X and Y chromosome

Table 2: Comparison of 47, XXY Klienfelter syndrome and 48, XXYY syndrome (Adapted from Tartaglia et al., 48, XXYY, 48, XXXY, and 49, XXXXY syndromes: Not just variants of Klinefelter syndrome, Acta Paediatr: 2011; 100(6):851-860) Characteristic features 47, XXY 48, XXYY Parent of origin of extra chromosomes 50% maternal and 50% paternal 100% paternal Prevalence 1:650-1:1,000 males 1:18,000-1:40,000 males Congenital malformations and common congenital Clinodactyly (70%) and congenital malformations malformations 18% (inguinal hernia, 56% (inguinal hernia, cardiac, radioulnar synostosis, cleft palate - occult, submucous) cleft palate, clubfoot, renal dysplasia) Developmental and cognitive Speech and motor delays (40-75%); Speech and motor delays (75-92%); 50-75% learning disabilities 100% learning disabilities

Journal of Conservative Dentistry | May-Jun 2015 | Vol 18 | Issue 3 267 Krishnamoorthy and Gopikrishna: Endodontic management of a hypertaurodontic tooth associated with 48, xxyy syndrome

This case showing 48, XXYY karyotype is recognized 12. Mednick GA. Two case reports: Taurodontism and taurodontism in Kleinfelter’s syndrome. J Mich Dent Assoc 1973;55:212-5. as a distinct clinical and genetic entity. This syndrome 13. Koshiba H, Kimura O, Nakata M. Witkop CJ Jr. Clinical, genetic, and was previously considered to be a variant of Klinefelter histologic features of the trichoonychodental (TOD) syndrome. Oral syndrome (47, XXY); however, it is now considered to be Surg Oral Med Oral Pathol 1978;46:376-85. 14. Jaspers MT. Taurodontism in the . Oral Surg Oral Med a distinct phenotype with more significant cognitive and Oral Pathol 1981;51:632-6. psychological impairments. The characteristic differences 15. Bassarelli V, Baccetti T, Bassarelli T, Franchi L. The dentomaxillofacial characteristics of the Prader-Labhart-Willi syndrome. A clinical case between these two syndromes have been well documented report. Minerva Stomatol 1991;40:811-9. by Tartaglia et al.,[27] and are highlighted in Table 2. 16. Tsai SJ, O’Donnell D. Dental findings in an adult with Lowe’s syndrome. Spec Care Dentist 1997;17:207-10. 17. Spangler GS, Hall KI, Kula K, Hart TC, Wright JT. Enamel structure and CONCLUSION composition in the tricho-dento-osseous syndrome. Connect Tissue Res 1998;39:165-75. 18. Breen GH. Taurodontism, an unreported dental finding in Wolf- Knowledge regarding 48, XXYY syndrome and its Hirschhorn (4p-) syndrome. ASDC J Dent Child 1998;65:344-5, 356. dentofacial manifestations is important for early diagnosis 19. Hunter ML, Roberts GJ. Oral and dental anomalies in Ellis van Creveld syndrome (chondroectodermal dysplasia): Report of a case. Int J and long-term predictable medical and dental health Paediatr Dent 1998;8:153-7. management. An early recognition of such a disorder is 20. Terezhalmy GT, Riley CK, Moore WS. Clinical images in oral medicine and maxillofacial radiology. Taurodontism. Quintessence Int 2001;32:254-5. crucial in improving the psychological as well a dental 21. Seymen F, Tuna B, Kayserili H. Seckel syndrome: Report of a case. J Clin quality of life in affected patients. Pediatr Dent 2002;26:305-9. 22. Akintoye SO, Lee JS, Feimster T, Booher S, Brahim J, Kingman A, et al. Dental characteristics of fibrous dysplasia and McCune-Albright syndrome. REFERENCES Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2003;96:275-82. 23. Ersin NK, Tugsel Z, Go¨kce B, Ozpinar B, Eronat N. Lenz microphthalmia 1. Peet J, Weaver DD, Vance GH. 49, XXXXY: A distinct phenotype. Three syndrome with dental anomalies: A case report. J Dent Child (Chic) new cases and review. J Med Genet 1998;35:420-4. 2003;70:262-5. 2. Tartaglia N, Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, 24. Petzold D, Kratzsch E, Opitz Ch, Tinschert S. The Kabuki syndrome: et al. A new look at XXXY syndrome: Medical and psychological features. Four patients with oral abnormalities. Eur J Orthod 2003;25:13-9. Am J Med Genet A 2008;146A:1509-22. 25. Axelsson S. Variability of the cranial and dental phenotype in Williams 3. Sorensen K, Nielsen J, Jacobsen P, Rolle T. The 48, XXYY syndrome. syndrome. Swed Dent J Suppl 2005:3-67. J Ment Defic Res 1978;22:197-205. 26. Tomona N, Smith AC, Guadagnini JP, Hart TC. Craniofacial and 4. Feichtinger C, Rossiwall B. Taurodontism in human sex chromosome dental phenotype of Smith-Magenis syndrome. Am J Med Genet A aneuploidy. Arch Oral Biol 1977;22:327-9. 2006;140:2556-61. 5. Goldstien E, Gottlieb MA. Taurodontism: Familial tendencies 27. Tartaglia N, Ayari N, Howell S, D’Epagnier C, Zeitler P. 48, XXYY, 48, XXXY demonstrated in eleven of fourteen case reports. Oral Surg Oral Med and 49, XXXXY syndromes: Not just variants of Klinefelter syndrome. Oral Pathol 1973;36:131-44. Acta Paediatr 2011;100:851-60. 6. Tsesis I, Shifman A, Kaufman AY. Taurodontism: An endodontic challenge. Report of a case. J Endod 2003;29:353-5. 7. Jafarzadeh H, Azarpazhooh A, Mayhall JT. Taurodontism: A review How to cite this article: Krishnamoorthy S, Gopikrishna V. of the condition and endodontic treatment challenges. Int Endod J 2008;41:375-88. Endodontic management of a hypertaurodontic tooth associated 8. Shaw JC. Taurodont teeth in South African races. J Anat 1928;62:476-98. with 48, XXYY syndrome: A review and case report. J Conserv 9. Gardner DG, Girgis SS. Taurodontism, shovel-shaped incisors and the Dent 2015;18:265-8. klinefelter syndrome. Dent J 1978;44:372-3. 10. MacDonald-Jankowski DS, Li TT. Taurodontism in a young adult Chinese population. Dentomaxillofac Radiol 1993;22:140-4. Source of Support: Nil, Confl ict of Interest: None declared. 11. Gorlin RJ. Thoma’s Oral Pathology. 6th ed. St. Louis: Mosby; 1970.

268 Journal of Conservative Dentistry | May-Jun 2015 | Vol 18 | Issue 3