A Case of Dentin Dysplasia with Full Mouth Rehabilitation: A 3-year Longitudinal Study.
Identifieur interne : 000B84 ( PubMed/Corpus ); précédent : 000B83; suivant : 000B85A Case of Dentin Dysplasia with Full Mouth Rehabilitation: A 3-year Longitudinal Study.
Auteurs : Suneet Khandelwal ; Dheeraj Gupta ; Lalit LikhyaniSource :
- International journal of clinical pediatric dentistry [ 0974-7052 ] ; 2014.
Abstract
Dentin dysplasia, a rare hereditary disorder of dentin formation, is characterized by normal enamel but atypical dentin formation along with abnormal pulpal morphology. It is inherited as an autosomal dominant trait. It has been divided into two clinical entities: type I (radicular) and type II (coronal). Early diagnosis and initiation of effective regular dental treatments may help the patients with this condition to delay or prevent the loss of the entire dentition and help them in cope up with edentulous state in early ages. The condition undoubtedly has a negative impact on the physical and psychological well-being of the affected individual. Numerous factors have to be considered during the prosthetic rehabilitation of patients with dentin dysplasia. Treatment protocol varies according to clinical case. Although literature reports suggest general guidelines for treatment planning, the present case report describes a full mouth rehabilitation of an 8-year-old female patient with dentin dysplasia. How to cite this article: Khandelwal S, Gupta D, Likhyani L. A Case of Dentin Dysplasia with Full Mouth Rehabilitation: A 3-year Longitudinal Study. Int J Clin Pediatr Dent 2014;7(2): 119-124.
DOI: 10.5005/jp-journals-10005-1248
PubMed: 25356011
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<front><div type="abstract" xml:lang="en">Dentin dysplasia, a rare hereditary disorder of dentin formation, is characterized by normal enamel but atypical dentin formation along with abnormal pulpal morphology. It is inherited as an autosomal dominant trait. It has been divided into two clinical entities: type I (radicular) and type II (coronal). Early diagnosis and initiation of effective regular dental treatments may help the patients with this condition to delay or prevent the loss of the entire dentition and help them in cope up with edentulous state in early ages. The condition undoubtedly has a negative impact on the physical and psychological well-being of the affected individual. Numerous factors have to be considered during the prosthetic rehabilitation of patients with dentin dysplasia. Treatment protocol varies according to clinical case. Although literature reports suggest general guidelines for treatment planning, the present case report describes a full mouth rehabilitation of an 8-year-old female patient with dentin dysplasia. How to cite this article: Khandelwal S, Gupta D, Likhyani L. A Case of Dentin Dysplasia with Full Mouth Rehabilitation: A 3-year Longitudinal Study. Int J Clin Pediatr Dent 2014;7(2): 119-124.</div>
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<Abstract><AbstractText>Dentin dysplasia, a rare hereditary disorder of dentin formation, is characterized by normal enamel but atypical dentin formation along with abnormal pulpal morphology. It is inherited as an autosomal dominant trait. It has been divided into two clinical entities: type I (radicular) and type II (coronal). Early diagnosis and initiation of effective regular dental treatments may help the patients with this condition to delay or prevent the loss of the entire dentition and help them in cope up with edentulous state in early ages. The condition undoubtedly has a negative impact on the physical and psychological well-being of the affected individual. Numerous factors have to be considered during the prosthetic rehabilitation of patients with dentin dysplasia. Treatment protocol varies according to clinical case. Although literature reports suggest general guidelines for treatment planning, the present case report describes a full mouth rehabilitation of an 8-year-old female patient with dentin dysplasia. How to cite this article: Khandelwal S, Gupta D, Likhyani L. A Case of Dentin Dysplasia with Full Mouth Rehabilitation: A 3-year Longitudinal Study. Int J Clin Pediatr Dent 2014;7(2): 119-124.</AbstractText>
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<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Ann Anat. 1999 Jan;181(1):138-40</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>J Dent Res. 2007 May;86(5):392-9</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Orphanet J Rare Dis. 2008 Nov 20;3:31</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Int J Paediatr Dent. 1999 Mar;9(1):37-42</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1998 Dec;86(6):733-7</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Oral Surg Oral Med Oral Pathol. 1991 Jul;72 (1):119-25</RefSource>
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