scholarly journals Editorial: Craniofacial Growth and Development: Novel Insights

Author(s):  
Erika Calvano Küchler ◽  
Rafaela Scariot ◽  
Christian Kirschneck
2017 ◽  
Vol 87 (6) ◽  
pp. 897-910 ◽  
Author(s):  
Kris Currie ◽  
Dena Sawchuk ◽  
Humam Saltaji ◽  
Heesoo Oh ◽  
Carlos Flores-Mir ◽  
...  

ABSTRACT Objective: To provide a synthesis of the published studies evaluating the natural growth and development of the human posterior cranial base (S-Ba). Materials and Methods: The search was performed on MEDLINE, Embase, PubMed, and all EBM Reviews electronic databases. In addition, reference lists of the included studies were hand-searched. Articles were included if they analyzed posterior cranial-base growth in humans specifically. Study selection, data extraction, and risk of bias assessment were completed in duplicate. A meta-analysis was not justified. Results: Finally, 23 published studies were selected: 5 cross-sectional and 18 cohort studies. Articles were published between 1955 and 2015, and all were published in English. The sample sizes varied between 20 and 397 individuals and consisted of craniofacial measurements from either living or deceased human skulls. Validity of the measurements was not determined in any of the studies, while six papers reported some form of reliability assessment. All the articles included multiple time points within the same population or data from multiple age groups. Growth of S-Ba was generally agreed to be from spheno-occipital synchondrosis growth. Basion displaced downward and backward and sella turcica moved downward and backward during craniofacial growth. Timing of cessation of S-Ba growth was not conclusive due to limited identified evidence. Conclusions: Current evidence suggests that S-Ba is not totally stable, as its dimensions change throughout craniofacial growth and a minor dimensional change is observed even in late adulthood.


2010 ◽  
Vol 10 (1) ◽  
pp. 18 ◽  
Author(s):  
Eric J Schmidt ◽  
Trish E Parsons ◽  
Heather A Jamniczky ◽  
Julian Gitelman ◽  
Cvett Trpkov ◽  
...  

2020 ◽  
Vol 34 (S1) ◽  
pp. 1-1
Author(s):  
Nandini Singh ◽  
Roger H. Reeves ◽  
Joan T. Richtsmeier

2010 ◽  
Vol 21 (3) ◽  
pp. 711-718 ◽  
Author(s):  
James Cray ◽  
Anne M. Burrows ◽  
Lisa Vecchione ◽  
Emily Lensie ◽  
Gary E. Decesare ◽  
...  

2009 ◽  
Vol 21 (2) ◽  
Author(s):  
Inne Suherna Sasmita ◽  
Arlette Suzy Puspa Pertiwi ◽  
M Harun Achmad

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 the oral manifestations associated with the craniofacial growth and development of Turner syndrome.


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