A copy of this work was available on the public web and has been preserved in the Wayback Machine. The capture dates from 2018; you can also visit the original URL.
The file type is application/pdf.
Craniofacial growth and development of Turner syndrome children
2009
Padjadjaran Journal of Dentistry
Preserved Fulltext
Turner syndrome is a genetic disorder which characterized by specific physical appearance and the lost of one of sex chromosome in females. The most frequent chromosome constitution in Turner syndrome is 45X. This disorder may cause an interruption of growth and development in the whole body as well as in the craniofacial region. The oral manifestations of Turner syndrome are micrognathia, high palate, malocclusion, and the premature eruption of first permanent molars. This paper will discuss
doi:10.24198/pjd.vol21no2.14104
fatcat:kspkolqaqfeh3b34gijbqp4voa