Dental Treatment of a Child with Pallister-Killian Syndrome

The Pallister-Killian syndrome (PKS) is an extremely rare genetic disorder with an incidence estimated around 1/25000. PKS is a multiple congenital anomaly deficit syndrome caused by mosaic tissue limited tetrasomy for chromosome 12p. The presented report is the first confirmed case with PKS in Turk...

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Detalles Bibliográficos
Autores principales: Didinen, Serhan, Atabek, Didem, Kip, Gülay, Patır Münevveroğlu, Aslı, Tulunoğlu, Özlem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779513/
https://www.ncbi.nlm.nih.gov/pubmed/26998367
http://dx.doi.org/10.1155/2016/4130961

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779513/
https://www.ncbi.nlm.nih.gov/pubmed/26998367
http://dx.doi.org/10.1155/2016/4130961

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