References
- Aldred MJ, Crawford PJ : Variable expression in Amelogenesis imperfecta with taurodontism. J Oral Pathol, 17:327-333, 1988. https://doi.org/10.1111/j.1600-0714.1988.tb01545.x
- Collins MA, Mauriello SM, Tyndall DA, Wright JT : Dental anomalies associated with amelogenesis imperfecta: a radiographic assessment. Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 88:358-364, 1999. https://doi.org/10.1016/S1079-2104(99)70043-0
- Ooya K, Nalbandian J, Noikura T : Autosomal recessive rough hypoplastic amelogenesis imperfecta. A case report with clinical, light microscopic, radiographic, and electron microscopic observations. Oral Surg Oral Med Oral Pathol, 65:449-458, 1988. https://doi.org/10.1016/0030-4220(88)90360-X
- Peters E, Cohen M, Altini M : Rough hypoplastic amelogenesis imperfecta with follicular hyperplasia. Oral Surg Oral Med Oral Pathol, 74:87-92, 1992. https://doi.org/10.1016/0030-4220(92)90220-K
- Parry DA, Mighell AJ, Inglehearn CF, et al. : Mutations in CNNM4 cause Jalili syndrome, consisting of autosomalrecessive cone-rod dystrophy and amelogenesis imperfecta. Am J Hum Genet, 84:266-273, 2009. https://doi.org/10.1016/j.ajhg.2009.01.009
- Ababneh FK, AlSwaid A, AlBalwi MA, et al. : Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome. Am J Med Genet A, 161:3155-3160, 2013. https://doi.org/10.1002/ajmg.a.36160
- Wright JT, Johnson LB, Fine JD : Development defects of enamel in humans with hereditary epidermolysis bullosa. Arch Oral Biol, 38:945-955, 1993. https://doi.org/10.1016/0003-9969(93)90107-W
- Wright JT, Hong SP, Luder HU, et al. : DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dentoosseous syndrome. Am J Med Genet A, 146:343-349, 2008. https://doi.org/10.1002/ajmg.a.32132
- O'Sullivan J, Bitu CC, Dixon MJ, et al. : Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome. Am J Hum Genet, 88:616-620, 2011. https://doi.org/10.1016/j.ajhg.2011.04.005
- MacGibbon D : Generalized enamel hypoplasia and renal dysfunction. Aust Dent J, 17:61-63, 1972. https://doi.org/10.1111/j.1834-7819.1972.tb02747.x
- Kala Vani SV, Varsha M, Sankar YU : Enamel renal syndrome: a rare case report. J Indian Soc Pedod Prev Dent, 30:169-172, 2012. https://doi.org/10.4103/0970-4388.100006
- Witkop CJ : Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol, 17:547-553, 1988. https://doi.org/10.1111/j.1600-0714.1988.tb01332.x
- Normand Tranchade I, Bonarek H, Nancy J, et al. : Amelogenesis imperfecta and nephrocalcinosis: a new case of this rare syndrome. J Clin Pediatr Dent, 27:171-175, 2003.
- Seow WK : Clinical diagnosis and management strategies of amelogenesis imperfectavariants. Pediatr Dent, 15:384-393, 1993.
- Feller L, Jadwat Y, Raubenheimer EJ, et al. : Enamel dysplasia with odontogenic fibroma-like hamartomas: review of the literature and report of a case. Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 101:620-624, 2006. https://doi.org/10.1016/j.tripleo.2005.06.015
- Kantaputra PN, Bongkochwilawan C, Chaisrisookumporn YN, et al. : Periodontal disease and FAM20A mutations. J Hum Genet, 62:679-686, 2017. https://doi.org/10.1038/jhg.2017.26
- Paula LM, Melo NS, Acevedo AC, et al. : Case report of a rare syndrome associating amelogenesis imperfecta and nephrocalcinosis in a consanguineous family. Arch Oral Biol, 50:237-242, 2005. https://doi.org/10.1016/j.archoralbio.2004.11.023
- Martelli-Junior H, Bonan PR, Coletta RD, et al. : Case reports of a new syndrome associating gingival fibromatosis and dental abnormalities in a consanguineous family. J Periodontol, 79:1287-1296, 2008. https://doi.org/10.1902/jop.2008.070520
- Yonemochi H, Noda T, Saku T : Pericoronal hamartomatous lesions in the opercula of teeth delayed in eruption: an immunohistochemical study of the extracellular matrix. J Oral Pathol Med, 27:441-452, 1998. https://doi.org/10.1111/j.1600-0714.1998.tb01982.x
- Cho YA, Yoon HJ, Hong SD, et al. : Multiple calcifying hyperplastic dental follicles: comparison with hyperplastic dental follicles. J Oral Pathol Med, 40:243-249, 2011. https://doi.org/10.1111/j.1600-0714.2010.00968.x
- O'Connell S, Davies J, Smallridge J, Vaidyanathan M : Amelogenesis imperfecta associated with dental follicular-like hamartomas and generalised gingival enlargement. Eur Arch Paediatr Dent, 15:361-368, 2014. https://doi.org/10.1007/s40368-013-0106-8
- Dure-Molla M, Quentric M, Bloch-Zupan A, et al. : Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations. Orphanet J Rare Dis, 9:84, 2014. https://doi.org/10.1186/1750-1172-9-84
- Wang SK, Aref P, Hu JC, et al. : FAM20A mutations can cause enamel-renal syndrome (ERS). PLoS Genet, 9:e1003302, 2013. https://doi.org/10.1371/journal.pgen.1003302
- Jaureguiberry G, Dure-Molla M, Kleta R, et al. : Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations. Nephron Physiol, 122:1-6, 2012. https://doi.org/10.1159/000349989
- Cho SH, Seymen F, Kim JW, et al. : Novel FAM20A mutations in hypoplastic amelogenesis imperfecta. Hum Mutat, 33:91-94, 2012. https://doi.org/10.1002/humu.21621
- Proctor, Kumar RN, Porter S, et al. : Oral and dental aspects of chronic renal failure. J Dent Res, 84:199-208, 2005. https://doi.org/10.1177/154405910508400301