File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Conference Paper: A case report of Pallister-Killian syndrome (PKS): newdental findings

TitleA case report of Pallister-Killian syndrome (PKS): newdental findings
Authors
Issue Date2009
PublisherWiley-Blackwell Publishing Ltd.. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=0960-7439
Citation
The 22nd Congress of the International Association of Paediatric Dentistry, Munich, Germany, 17-20 June 2009. In International Journal of Paediatric Dentistry, 2009, v. 19 n. S1, p. 140 How to Cite?
AbstractIntroduction: Pallister-Killian syndrome (PKS) is a sporadic con-dition with autosomic tetrasomy of chromosome 12 p, resulting ina mosaic distribution of the supernumerary isochromosome. Wereport a case of PKS affecting an 11-year-old girl with 12 pmosaicism (karyotype 46, XX). Diagnosis was confirmed at 2 yearsof age. She presented with alopecia, dysmorphic facies, diaphrag-matic hernia, PDA and a dilated aorta root. Extra-oral findingsincluded facial asymmetry, low implantation of the ears and sparseeyebrows. The dental findings included delayed eruption, macr-odont maxillary right central incisor (or double tooth) withcongenital absence of the lateral incisor in both the primary andpermanent dentitions. There was an anterior single tooth crossbite,spacing, and a posterior cross-bite.Clinical management: The discrepancy in size between the maxil-lary permanent right and left central incisors presented a treatmentdilemma, because reduction of right central incisor was impracti-cal, so the left central incisor was built up to improve the aestheticsof the anterior region. All of the invasive procedures wereperformed under prophylactic antibiotic cover according to theadvice of her paediatrician. Due to her delayed dental develop-ment, orthodontic treatment has not yet been carried out.Conclusion: In PKS dental anomalies, such as macrodontia, maybe present. The management of this anomaly should be cognisantof the systemic problems and yet able to provide an aestheticoutcome.
Persistent Identifierhttp://hdl.handle.net/10722/61355
ISSN
2015 Impact Factor: 1.303
2015 SCImago Journal Rankings: 0.721

 

DC FieldValueLanguage
dc.contributor.authorDu, RY-
dc.contributor.authorChung, CWM-
dc.contributor.authorKing, NM-
dc.date.accessioned2010-07-13T03:37:52Z-
dc.date.available2010-07-13T03:37:52Z-
dc.date.issued2009-
dc.identifier.citationThe 22nd Congress of the International Association of Paediatric Dentistry, Munich, Germany, 17-20 June 2009. In International Journal of Paediatric Dentistry, 2009, v. 19 n. S1, p. 140-
dc.identifier.issn0960-7439-
dc.identifier.urihttp://hdl.handle.net/10722/61355-
dc.description.abstractIntroduction: Pallister-Killian syndrome (PKS) is a sporadic con-dition with autosomic tetrasomy of chromosome 12 p, resulting ina mosaic distribution of the supernumerary isochromosome. Wereport a case of PKS affecting an 11-year-old girl with 12 pmosaicism (karyotype 46, XX). Diagnosis was confirmed at 2 yearsof age. She presented with alopecia, dysmorphic facies, diaphrag-matic hernia, PDA and a dilated aorta root. Extra-oral findingsincluded facial asymmetry, low implantation of the ears and sparseeyebrows. The dental findings included delayed eruption, macr-odont maxillary right central incisor (or double tooth) withcongenital absence of the lateral incisor in both the primary andpermanent dentitions. There was an anterior single tooth crossbite,spacing, and a posterior cross-bite.Clinical management: The discrepancy in size between the maxil-lary permanent right and left central incisors presented a treatmentdilemma, because reduction of right central incisor was impracti-cal, so the left central incisor was built up to improve the aestheticsof the anterior region. All of the invasive procedures wereperformed under prophylactic antibiotic cover according to theadvice of her paediatrician. Due to her delayed dental develop-ment, orthodontic treatment has not yet been carried out.Conclusion: In PKS dental anomalies, such as macrodontia, maybe present. The management of this anomaly should be cognisantof the systemic problems and yet able to provide an aestheticoutcome.-
dc.languageeng-
dc.publisherWiley-Blackwell Publishing Ltd.. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=0960-7439-
dc.relation.ispartofInternational Journal of Paediatric Dentistry-
dc.rightsPreprint This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article]. Authors are not required to remove preprints posted prior to acceptance of the submitted version. Postprint This is the accepted version of the following article: [full citation], which has been published in final form at [Link to final article].-
dc.titleA case report of Pallister-Killian syndrome (PKS): newdental findings-
dc.typeConference_Paper-
dc.identifier.emailKing, NM: hhdbknm@HKUCC.hku.hk-
dc.identifier.authorityKing, NM=rp00006-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1111/j.1365-263X.2009.00993_17.x-
dc.identifier.hkuros161647-
dc.identifier.volume19-
dc.identifier.issueS1-
dc.identifier.spage140-
dc.identifier.epage140-
dc.publisher.placeUnited Kingdom-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats