Literature DB >> 26032705

Dental management of Rothmund-Thomson syndrome with partial anodontia.

Nilesh Vithaldas Rathi1, Mayur Shrigopal Bhattad2, Nilima Thosar1, Sudhindra Baliga1.   

Abstract

Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive trait disease. It is characterised by skin, eye and skeletal abnormalities. Abnormalities associated with teeth include abnormal crown and root formations, rudimentary or hypoplastic teeth, microdontia and multiple missing teeth. In the present case, there were multiple decayed primary teeth and multiple congenitally missing permanent teeth. Mandibular left primary first molar (tooth 74) was pulpally involved and obturated with mineral trioxide ggregate. Follow-up after 2 years revealed successful obturation. 2015 BMJ Publishing Group Ltd.

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Mesh:

Year:  2015        PMID: 26032705      PMCID: PMC4460316          DOI: 10.1136/bcr-2015-209994

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  15 in total

Review 1.  Rothmund-Thomson syndrome: review of the world literature.

Authors:  E M Vennos; M Collins; W D James
Journal:  J Am Acad Dermatol       Date:  1992-11       Impact factor: 11.527

2.  Usage of white mineral trioxide aggregate in a non-vital primary molar with no permanent successor.

Authors:  E Sen Tunc; S Bayrak
Journal:  Aust Dent J       Date:  2010-03       Impact factor: 2.291

Review 3.  Short root anomaly associated with Rothmund-Thomson syndrome.

Authors:  Tina D Roinioti; Panagiotis K Stefanopoulos
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod       Date:  2006-10-24

4.  Obturation of a retained primary mandibular second molar using mineral trioxide aggregate: a case report.

Authors:  S M O'Sullivan; G R Hartwell
Journal:  J Endod       Date:  2001-11       Impact factor: 4.171

5.  Variable presentation of Rothmund-Thomson syndrome.

Authors:  L A Pujol; R P Erickson; R A Heidenreich; C Cunniff
Journal:  Am J Med Genet       Date:  2000-11-27

6.  Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients.

Authors:  L L Wang; M L Levy; R A Lewis; M M Chintagumpala; D Lev; M Rogers; S E Plon
Journal:  Am J Med Genet       Date:  2001-07-22

7.  Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and products.

Authors:  S Kitao; N M Lindor; M Shiratori; Y Furuichi; A Shimamoto
Journal:  Genomics       Date:  1999-11-01       Impact factor: 5.736

8.  Physicochemical basis of the biologic properties of mineral trioxide aggregate.

Authors:  N K Sarkar; R Caicedo; P Ritwik; R Moiseyeva; I Kawashima
Journal:  J Endod       Date:  2005-02       Impact factor: 4.171

9.  Rothmund-Thomson syndrome with herpes encephalitis.

Authors:  T Ito; Y Tokura; S Moriwaki; K Yasuda; A Ohnishi; F Furukawa; K Yamaizumi; M Takigawa
Journal:  Eur J Dermatol       Date:  1999 Jul-Aug       Impact factor: 3.328

10.  Rothmund's syndrome; Thomson's syndrome; congenital poikiloderma with or without juvenile cataracts.

Authors:  W B TAYLOR
Journal:  AMA Arch Derm       Date:  1957-02
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