Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report

Sushmini Hegde; Hemcle Shalma Ganesan; Karidhi Sudesh Suraj

doi:doi:10.11648/j.ijdm.20180401.16

| Peer-Reviewed

Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report

Sushmini Hegde, Hemcle Shalma Ganesan, Karidhi Sudesh Suraj

Published in International Journal of Dental Medicine (Volume 4, Issue 1)

Received: 23 July 2018 Accepted: 9 August 2018 Published: 5 September 2018

Views: Downloads:

Download PDF

Share This Article

Twitter
Linked In
Facebook

Abstract

Amelogenesis imperfecta (AI) is a developmental disorder of genomic origin associated with structural enamel formation. Hereditary brown enamel, hereditary enamel dysplasia, hereditary brown opalescent teeth are the other terminologies used for AI. The prevalence varies from 1:700 to 1:14 000, according to the populations studied. AI affects the entire ectodermal component and the enamel may be hypoplastic, hypomineralized or both and affected teeth may be esthetically and functionally compromised, discolored, sensitive or prone to disintegration, leading to loss of occlusal vertical dimensions and very poor aesthetics. Although AI is considered as a single disease entity, it actually represents a group of heterogenous conditions, with diverse structural defects of enamel resulting in a range of clinical phenotypes. It is characterized by clinical and genetic heterogeneity in the absence of systemic abnormalities or diseases. AI had been found to be associated with non-enamel anomalies such as delayed eruption, crown resorption, congenitally missing teeth, pulpal calcifications, dental follicular hamartomas, and gingival hyperplasia. Mutations in the amelogenin, enamelin, and kallikrein-4 genes have been demonstrated to different types of AI.Restoration of the dentition poses a great challenge when all the teeth are severely affected. The treatment opportunities for these patients may help in refining their lifestyle. This case report reviews a holistic multidisciplinary treatment approach for the oral rehabilitation of patient with hypoplastic AI with multiple impacted teeth.

Published in	International Journal of Dental Medicine (Volume 4, Issue 1)
DOI	10.11648/j.ijdm.20180401.16
Page(s)	27-30
Creative Commons	This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.
Copyright	Copyright © The Author(s), 2018. Published by Science Publishing Group

Keywords

Amelogenesis Imperfecta, Hypoplastic, Impacted Teeth

References

[1]	Backmon.B. Inherited enamel defects. Ciba Found symp. 1997; 205:175-182.
[2]	Aldred M.J, Crawford P.J. AmelogenesisImperfecta; towards a new classification. Oral Dis.1995;1:2-5.
[3]	Collins MA et al. Dental anomalies associated with amelogenesisimperfecta: A radiographic assessment. Oral Surg Oral Med Oral Pathol Oral RadiolEndod 1999; 88:358-64.
[4]	Peter T, Titus S, Francis G. Full mouth rehabilitation of a case with amelogenesisimperfecta. SRM University Journal of Dental Sciences; 2010: 1(3).
[5]	Shetty YB, Shetty A. Oral Rehabilitation of a Young Adult with AmelogenesisImperfecta: a case report. J Indian ProsthodontSoc; 2010; 10(4):240–245.
[6]	WitkopJr CJ, Kuhlmann W, Sauk J. Autosomal recessive pigmented hypomaturationamelogenesisimperfecta. Report of a kindred. Oral Surg Oral Med Oral Pathol.1973;36:367–382.
[7]	Sengün A, Özer F. Restoring function and esthetics in a patient with amelogenesisimperfecta: a case report. QuintessenceInt2002;33:199–204.
[8]	Fischman SL, Fischman BC. Hypoplasticamelogenesisimperfecta: report of case. J Am Dent Assoc1967;75:929–931Reddy S, Nisha V, Harish BN. Hypoplasticamelogenesisimperfecta with multiple impacted teeth – report of two cases. J ClinExp Dent. 2010; 2(4):e207-11.
[9]	Moretti. A.B.S, Sakai.V.T, Oliveira.T.M Oral management of a child with mixed dentition affected by AmelogenesisImperfecta. Journal of Dentistry for Children. 2007; 74(2):157-160.
[10]	Begum N, Bhandarkar GP, Kini R, Naik V, Rashmi K, D Souza LC. AmelogenesisImperfecta: A Series of Case Report. Int J Adv Health Sci 2015;2(1):17-21.
[11]	Koruyucu M, Bayram M, Tuna EB, Gencay K, Seymen F. Clinical findings and long-term managements of patients with amelogenesisimperfecta. Eur J Dent 2014; 8:546-52.
[12]	Mehta DN, Shah J, Thakkar B. AmelogenesisImperfecta: four case reports. J Nat SciBiol Med 2013 Jul-Dec;4(2):462-465.

Cite This Article

Plain Text BibTeX RIS

APA Style

Sushmini Hegde, Hemcle Shalma Ganesan, Karidhi Sudesh Suraj. (2018). Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report. International Journal of Dental Medicine, 4(1), 27-30. https://doi.org/10.11648/j.ijdm.20180401.16

Copy | Download

ACS Style

Sushmini Hegde; Hemcle Shalma Ganesan; Karidhi Sudesh Suraj. Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report. Int. J. Dent. Med. 2018, 4(1), 27-30. doi: 10.11648/j.ijdm.20180401.16

Copy | Download

AMA Style

Sushmini Hegde, Hemcle Shalma Ganesan, Karidhi Sudesh Suraj. Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report. Int J Dent Med. 2018;4(1):27-30. doi: 10.11648/j.ijdm.20180401.16

Copy | Download

@article{10.11648/j.ijdm.20180401.16,
  author = {Sushmini Hegde and Hemcle Shalma Ganesan and Karidhi Sudesh Suraj},
  title = {Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report},
  journal = {International Journal of Dental Medicine},
  volume = {4},
  number = {1},
  pages = {27-30},
  doi = {10.11648/j.ijdm.20180401.16},
  url = {https://doi.org/10.11648/j.ijdm.20180401.16},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijdm.20180401.16},
  abstract = {Amelogenesis imperfecta (AI) is a developmental disorder of genomic origin associated with structural enamel formation. Hereditary brown enamel, hereditary enamel dysplasia, hereditary brown opalescent teeth are the other terminologies used for AI. The prevalence varies from 1:700 to 1:14 000, according to the populations studied. AI affects the entire ectodermal component and the enamel may be hypoplastic, hypomineralized or both and affected teeth may be esthetically and functionally compromised, discolored, sensitive or prone to disintegration, leading to loss of occlusal vertical dimensions and very poor aesthetics. Although AI is considered as a single disease entity, it actually represents a group of heterogenous conditions, with diverse structural defects of enamel resulting in a range of clinical phenotypes. It is characterized by clinical and genetic heterogeneity in the absence of systemic abnormalities or diseases. AI had been found to be associated with non-enamel anomalies such as delayed eruption, crown resorption, congenitally missing teeth, pulpal calcifications, dental follicular hamartomas, and gingival hyperplasia. Mutations in the amelogenin, enamelin, and kallikrein-4 genes have been demonstrated to different types of AI.Restoration of the dentition poses a great challenge when all the teeth are severely affected. The treatment opportunities for these patients may help in refining their lifestyle. This case report reviews a holistic multidisciplinary treatment approach for the oral rehabilitation of patient with hypoplastic AI with multiple impacted teeth.},
 year = {2018}
}

Copy | Download

TY  - JOUR
T1  - Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report
AU  - Sushmini Hegde
AU  - Hemcle Shalma Ganesan
AU  - Karidhi Sudesh Suraj
Y1  - 2018/09/05
PY  - 2018
N1  - https://doi.org/10.11648/j.ijdm.20180401.16
DO  - 10.11648/j.ijdm.20180401.16
T2  - International Journal of Dental Medicine
JF  - International Journal of Dental Medicine
JO  - International Journal of Dental Medicine
SP  - 27
EP  - 30
PB  - Science Publishing Group
SN  - 2472-1387
UR  - https://doi.org/10.11648/j.ijdm.20180401.16
AB  - Amelogenesis imperfecta (AI) is a developmental disorder of genomic origin associated with structural enamel formation. Hereditary brown enamel, hereditary enamel dysplasia, hereditary brown opalescent teeth are the other terminologies used for AI. The prevalence varies from 1:700 to 1:14 000, according to the populations studied. AI affects the entire ectodermal component and the enamel may be hypoplastic, hypomineralized or both and affected teeth may be esthetically and functionally compromised, discolored, sensitive or prone to disintegration, leading to loss of occlusal vertical dimensions and very poor aesthetics. Although AI is considered as a single disease entity, it actually represents a group of heterogenous conditions, with diverse structural defects of enamel resulting in a range of clinical phenotypes. It is characterized by clinical and genetic heterogeneity in the absence of systemic abnormalities or diseases. AI had been found to be associated with non-enamel anomalies such as delayed eruption, crown resorption, congenitally missing teeth, pulpal calcifications, dental follicular hamartomas, and gingival hyperplasia. Mutations in the amelogenin, enamelin, and kallikrein-4 genes have been demonstrated to different types of AI.Restoration of the dentition poses a great challenge when all the teeth are severely affected. The treatment opportunities for these patients may help in refining their lifestyle. This case report reviews a holistic multidisciplinary treatment approach for the oral rehabilitation of patient with hypoplastic AI with multiple impacted teeth.
VL  - 4
IS  - 1
ER  -

Copy | Download

Author Information

Sushmini Hegde

Department of Oral Medicine and Radiology, the Oxford Dental College and Hospital, Bengaluru, India
Hemcle Shalma Ganesan

Department of Oral Medicine and Radiology, the Oxford Dental College and Hospital, Bengaluru, India
Karidhi Sudesh Suraj

Department of Prosthodontics and Crown and Bridge, the Oxford Dental College and Hospital, Bengaluru, India

Download PDF

Sections

Plain Text BibTeX RIS

APA Style

Sushmini Hegde, Hemcle Shalma Ganesan, Karidhi Sudesh Suraj. (2018). Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report. International Journal of Dental Medicine, 4(1), 27-30. https://doi.org/10.11648/j.ijdm.20180401.16

Copy | Download

ACS Style

Sushmini Hegde; Hemcle Shalma Ganesan; Karidhi Sudesh Suraj. Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report. Int. J. Dent. Med. 2018, 4(1), 27-30. doi: 10.11648/j.ijdm.20180401.16

Copy | Download

AMA Style

Sushmini Hegde, Hemcle Shalma Ganesan, Karidhi Sudesh Suraj. Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report. Int J Dent Med. 2018;4(1):27-30. doi: 10.11648/j.ijdm.20180401.16

Copy | Download

@article{10.11648/j.ijdm.20180401.16,
  author = {Sushmini Hegde and Hemcle Shalma Ganesan and Karidhi Sudesh Suraj},
  title = {Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report},
  journal = {International Journal of Dental Medicine},
  volume = {4},
  number = {1},
  pages = {27-30},
  doi = {10.11648/j.ijdm.20180401.16},
  url = {https://doi.org/10.11648/j.ijdm.20180401.16},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijdm.20180401.16},
  abstract = {Amelogenesis imperfecta (AI) is a developmental disorder of genomic origin associated with structural enamel formation. Hereditary brown enamel, hereditary enamel dysplasia, hereditary brown opalescent teeth are the other terminologies used for AI. The prevalence varies from 1:700 to 1:14 000, according to the populations studied. AI affects the entire ectodermal component and the enamel may be hypoplastic, hypomineralized or both and affected teeth may be esthetically and functionally compromised, discolored, sensitive or prone to disintegration, leading to loss of occlusal vertical dimensions and very poor aesthetics. Although AI is considered as a single disease entity, it actually represents a group of heterogenous conditions, with diverse structural defects of enamel resulting in a range of clinical phenotypes. It is characterized by clinical and genetic heterogeneity in the absence of systemic abnormalities or diseases. AI had been found to be associated with non-enamel anomalies such as delayed eruption, crown resorption, congenitally missing teeth, pulpal calcifications, dental follicular hamartomas, and gingival hyperplasia. Mutations in the amelogenin, enamelin, and kallikrein-4 genes have been demonstrated to different types of AI.Restoration of the dentition poses a great challenge when all the teeth are severely affected. The treatment opportunities for these patients may help in refining their lifestyle. This case report reviews a holistic multidisciplinary treatment approach for the oral rehabilitation of patient with hypoplastic AI with multiple impacted teeth.},
 year = {2018}
}

Copy | Download

TY  - JOUR
T1  - Amelogenesis Imperfecta, HypoplasticType with Multiple Impacted Teeth – A Case Report
AU  - Sushmini Hegde
AU  - Hemcle Shalma Ganesan
AU  - Karidhi Sudesh Suraj
Y1  - 2018/09/05
PY  - 2018
N1  - https://doi.org/10.11648/j.ijdm.20180401.16
DO  - 10.11648/j.ijdm.20180401.16
T2  - International Journal of Dental Medicine
JF  - International Journal of Dental Medicine
JO  - International Journal of Dental Medicine
SP  - 27
EP  - 30
PB  - Science Publishing Group
SN  - 2472-1387
UR  - https://doi.org/10.11648/j.ijdm.20180401.16
AB  - Amelogenesis imperfecta (AI) is a developmental disorder of genomic origin associated with structural enamel formation. Hereditary brown enamel, hereditary enamel dysplasia, hereditary brown opalescent teeth are the other terminologies used for AI. The prevalence varies from 1:700 to 1:14 000, according to the populations studied. AI affects the entire ectodermal component and the enamel may be hypoplastic, hypomineralized or both and affected teeth may be esthetically and functionally compromised, discolored, sensitive or prone to disintegration, leading to loss of occlusal vertical dimensions and very poor aesthetics. Although AI is considered as a single disease entity, it actually represents a group of heterogenous conditions, with diverse structural defects of enamel resulting in a range of clinical phenotypes. It is characterized by clinical and genetic heterogeneity in the absence of systemic abnormalities or diseases. AI had been found to be associated with non-enamel anomalies such as delayed eruption, crown resorption, congenitally missing teeth, pulpal calcifications, dental follicular hamartomas, and gingival hyperplasia. Mutations in the amelogenin, enamelin, and kallikrein-4 genes have been demonstrated to different types of AI.Restoration of the dentition poses a great challenge when all the teeth are severely affected. The treatment opportunities for these patients may help in refining their lifestyle. This case report reviews a holistic multidisciplinary treatment approach for the oral rehabilitation of patient with hypoplastic AI with multiple impacted teeth.
VL  - 4
IS  - 1
ER  -

Copy | Download