Letter to Editor- Oligodontia in Non-syndromic Children: Series of Three Cases

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Non Syndromic Oligodontia: Case Report

Oligodontia is a rare genetic disorder which represents the congenital absence of more than six teeth in primary, permanent or both dentitions. It is usually a part of a syndrome and seldom occurs as an isolated entity. Genes responsible for non syndromic oligodontia are found to be MSX1 and PAX9 genes. In this case report a 13 year old boy is presented who had absence of all four second perman...

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Multidisciplinary treatment of non-syndromic oligodontia

Oligodontia is the agenesis of 6 or more teeth, excluding third molars. The etiology of congenital absence of teeth is believed to be rooted in heredity or developmental anomalies. The absence of teeth in patients can cause aesthetic, functional, and psychological problems, particularly if the anterior region is involved. This case report describes the multidisciplinary treatment approach towar...

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Non-syndromic oligodontia: a case report.

BACKGROUND oligodontia is a condition with developmental absence of six or more permanent teeth excluding the third molars. It is a rare finding which has not been frequently documented in Nigerian children. OBJECTIVE to report a case of non syndromic oligodontia. METHODS The details of the clinical presentation, course and outcome of a 9-year-old child with oligodontia were reviewed. The c...

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Letter to editor

This article has no abstract.

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Letter to Editor

Dear Editor On September 2018, a case report titled “Squamous cell carcinoma arising from a sebaceous cyst” was published in the “Journal of Surgery and Trauma” (volume 6, issue 2) (1). It was an interesting article; however, I think when dealing about such rare tumors, it is important to be aware of other diseases, such as proliferating trichilemmal cysts (PTC) that may be confused with squam...

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ژورنال

عنوان ژورنال: JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH

سال: 2019

ISSN: 2249-782X

DOI: 10.7860/jcdr/2019/41315.13018