Dentin dysplasia type 1 - clinical management dilemmas: A case report of first-generation sufferers
Dentine Dysplasia is a rare genetic condition. The treatment options and dilemmas associated with the condition remain undiscovered so far. This article highlights the variations in traits and challenges faced in the treatment of the cases.
Main Authors: | Navneet Grewal, Samita Gumber, Anupam Kaur, Nirapjeet Kaur |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2018-01-01
|
Series: | Journal of Indian Society of Pedodontics and Preventive Dentistry |
Subjects: | |
Online Access: | http://www.jisppd.com/article.asp?issn=0970-4388;year=2018;volume=36;issue=2;spage=213;epage=215;aulast=Grewal |
Similar Items
-
Dentin dysplasia type 1 - Clinical management dilemmas: A case report of first-generation sufferers
by: Grewal, N., et al.
Published: (2018) -
Dentinal dysplasia type I: two cases in one family
by: Shahrabi M, et al.
Published: (2002-06-01) -
Rootless teeth: Dentin dysplasia type I
by: Sangamesh G Fulari, et al.
Published: (2013-01-01) -
An unusual variation of radicular dentin dysplasia: A rare case report with review of literature
by: Arun K Patnana, et al.
Published: (2020-01-01) -
Dentin dysplasia type II: An exclusive report of two cases in siblings
by: Deepak Daryani, et al.
Published: (2017-01-01)