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BMJ Case Rep ; 20152015 Jun 01.
Article in English | MEDLINE | ID: mdl-26032705

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.


Subject(s)
Anodontia/complications , Anodontia/therapy , Rothmund-Thomson Syndrome/complications , Rothmund-Thomson Syndrome/therapy , Child , Dental Caries/complications , Dental Caries/therapy , Diagnosis, Differential , Follow-Up Studies , Humans , Male , Rothmund-Thomson Syndrome/diagnosis , Tooth Abnormalities/complications , Tooth Abnormalities/therapy
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