Clinical manifestation of blepharocheilodontic (BCD) syndrome: a case review
BCD syndrome is a rare birth syndrome characterised by cleft lip and palate, euryblepharon with/without limb anomalies, ectropion of lower eyelids and hypertelorism. The dental anomalies include cone shaped microdontic teeth and oligodontia. Different combinations of these signs have been found spor...
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Universiti Kebangsaan Malaysia
2013
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my-ukm.journal.57092016-12-14T06:39:16Z http://journalarticle.ukm.my/5709/ Clinical manifestation of blepharocheilodontic (BCD) syndrome: a case review Navasheilla Retna .R, Sockalingam .S.N.M.P, BCD syndrome is a rare birth syndrome characterised by cleft lip and palate, euryblepharon with/without limb anomalies, ectropion of lower eyelids and hypertelorism. The dental anomalies include cone shaped microdontic teeth and oligodontia. Different combinations of these signs have been found sporadically in patients. This syndrome is also known as Elschnig’s syndrome. By at large, patients with this syndrome have no potentially fatal anomalies. Their growth and development were usually normal. This case review described the clinical manifestation and oral findings of a patient with BCD syndrome. The dental need of the patient was outlined. Universiti Kebangsaan Malaysia 2013-01 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/5709/1/14%2520R.%2520Navasheilla.pdf Navasheilla Retna .R, and Sockalingam .S.N.M.P, (2013) Clinical manifestation of blepharocheilodontic (BCD) syndrome: a case review. Sains Malaysiana, 42 (1). pp. 85-88. ISSN 0126-6039 http://www.ukm.my/jsm/ |
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BCD syndrome is a rare birth syndrome characterised by cleft lip and palate, euryblepharon with/without limb anomalies, ectropion of lower eyelids and hypertelorism. The dental anomalies include cone shaped microdontic teeth and oligodontia. Different combinations of these signs have been found sporadically in patients. This syndrome is also known as Elschnig’s syndrome. By at large, patients with this syndrome have no potentially fatal anomalies. Their growth and development were usually normal. This case review described the clinical manifestation and oral findings of a patient with BCD syndrome. The dental need of the patient was outlined. |
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Article |
author |
Navasheilla Retna .R, Sockalingam .S.N.M.P, |
spellingShingle |
Navasheilla Retna .R, Sockalingam .S.N.M.P, Clinical manifestation of blepharocheilodontic (BCD) syndrome: a case review |
author_facet |
Navasheilla Retna .R, Sockalingam .S.N.M.P, |
author_sort |
Navasheilla Retna .R, |
title |
Clinical manifestation of blepharocheilodontic (BCD) syndrome: a case review |
title_short |
Clinical manifestation of blepharocheilodontic (BCD) syndrome: a case review |
title_full |
Clinical manifestation of blepharocheilodontic (BCD) syndrome: a case review |
title_fullStr |
Clinical manifestation of blepharocheilodontic (BCD) syndrome: a case review |
title_full_unstemmed |
Clinical manifestation of blepharocheilodontic (BCD) syndrome: a case review |
title_sort |
clinical manifestation of blepharocheilodontic (bcd) syndrome: a case review |
publisher |
Universiti Kebangsaan Malaysia |
publishDate |
2013 |
url |
http://journalarticle.ukm.my/5709/1/14%2520R.%2520Navasheilla.pdf http://journalarticle.ukm.my/5709/ http://www.ukm.my/jsm/ |
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