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Dental Treatment of a Child with Pallister-Killian Syndrome: Critical Research | Chapter 10 | Innovations in Medicine and Medical Research Vol.2

The Pallister-Killian syndrome (PKS) is an extremely rare genetic disorder with an incidence estimated around 1/25000 and 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 Turkey. This report focuses on the orofacial clinical manifestations of an 6-year-old boy with PKS who was referred to the Department of Paediatric Dentistry clinic, Gazi University. It has been learned that the PKS was diagnosed 1 year after birth. Due to intellectual disability, it was decided to make the dental treatments under moderate sedation. Although significant tongue thrust and anterior open bite were determined, any oral appliances could not be applied because of the 2 epilepsy seizures in the last 2 years. The aim was to treat decayed teeth and set good oral hygiene in the patient’s mouth. Still, there is a probability for epilepsy seizures. If epileptic seizures stop permanently, we can apply an oral appliance to block tongue thrust. The patient is now under control. In cases of systemic and oral findings such as PKS, conducting medical and dental approaches together will increase the life quality of patients.
Author(s) Details

Serhan Didinen
Department of Pediatric Dentistry, Faculty of Dentistry, Istanbul Medipol University, Turkey.


Didem Atabek
Department of Pediatric Dentistry, Faculty of Dentistry, Gazi University, Turkey.


Dr. Gülay Kip

Department of Pediatric Dentistry, Faculty of Dentistry, Gazi University, Turkey and Department of Anesthesia and Reanimation, Faculty of Medicine, Gazi University, Turkey


Asli Patir Münevveroglu 
Department of Pediatric Dentistry, Faculty of Dentistry, Istanbul Medipol University, Turkey.

View Book: - http://bp.bookpi.org/index.php/bpi/catalog/book/161


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