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Cleidocranial Dysplasia - A case report

Cleidocranial Dysplasia - A case report J. Academy Adv Dental Research CASE REPORT All Rights Res E Siva Prasad Reddy* *M.D.S, Professor & Head, Department of Oral Medicine & Radiology, Teerthankar Mahaveer Dental College, Moradabad, Uttar Pradesh, India. Email:dr.espreddy@gmail.com Abstract: into osteoblasts[6,7]. Runx2, also known as OSH2, Cleidocranial dysplasia is an autosomal Cbfa1, PEBP2aA, AML-3 belongs to runt domain gene family [7.8]. In this article, we present a case dominant disorder with skeletal dysplasia. The dental manifestations are mainly delayed report of a child with the classical features of exfoliation of primary teeth and delayed eruption cleidocranial dysplasia. The pathology is due to an early development disorder of mesenchyme or of permanent teeth with multiple impacted supernumeraries, it is noteworthy that the case of connective tissue, causing retarded ossification of 20 year old girl reported here concerns the dental bone precursors, especially at junctions, which can lead to defective ossification or even failure of surgeon as it deals with high number of impacted and supernumerary teeth as well as unusual ossification of portions of skeletal structures. The findings such as Brachycephaly, frontal bossing, syndesmosis between cranial bones and the hypermobility of shoulders. symphysis of other bones are basically connective Keywords: Cleidocranial dysplasia, multiple tissue junctions. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of Advanced Oral Research SAGE

Cleidocranial Dysplasia - A case report

Reddy, E Siva Prasad
Journal of Advanced Oral Research , Volume 2 (2): 4 – May 1, 2011
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Publisher
SAGE
Copyright
© 2011 Academy of Advanced Dental Research
ISSN
2320-2068
eISSN
2320-2076
DOI
10.1177/2229411220110207
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Abstract

J. Academy Adv Dental Research CASE REPORT All Rights Res E Siva Prasad Reddy* *M.D.S, Professor & Head, Department of Oral Medicine & Radiology, Teerthankar Mahaveer Dental College, Moradabad, Uttar Pradesh, India. Email:dr.espreddy@gmail.com Abstract: into osteoblasts[6,7]. Runx2, also known as OSH2, Cleidocranial dysplasia is an autosomal Cbfa1, PEBP2aA, AML-3 belongs to runt domain gene family [7.8]. In this article, we present a case dominant disorder with skeletal dysplasia. The dental manifestations are mainly delayed report of a child with the classical features of exfoliation of primary teeth and delayed eruption cleidocranial dysplasia. The pathology is due to an early development disorder of mesenchyme or of permanent teeth with multiple impacted supernumeraries, it is noteworthy that the case of connective tissue, causing retarded ossification of 20 year old girl reported here concerns the dental bone precursors, especially at junctions, which can lead to defective ossification or even failure of surgeon as it deals with high number of impacted and supernumerary teeth as well as unusual ossification of portions of skeletal structures. The findings such as Brachycephaly, frontal bossing, syndesmosis between cranial bones and the hypermobility of shoulders. symphysis of other bones are basically connective Keywords: Cleidocranial dysplasia, multiple tissue junctions.

Journal

Journal of Advanced Oral Research – SAGE

Published: May 1, 2011

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