Q75.0
Conditions
Interventions
Group 1: children with non-syndromal craniosynostosis
Group 2: healthy children without craniosynostosis
Sponsors
Klinik und Poliklinik für Mund-, Kiefer - und Plastische Gesichtschirurgie
Eligibility
Sex/Gender
All
Age
3 Months to 4 Years
Inclusion criteria
Inclusion criteria: Arm1: non syndromal craniosynostosis without systemic disease Arm2: healthy children with normal maximal head circumference and a inconspicuous patiens`s history
Exclusion criteria
Exclusion criteria: children older 14 years, syndromal craniosynostosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| According to the database protocol a three-dimensional light optical scan with detailed morphometric and volumetric evaluation should be obtained in 10 patients preoperatively (at the age of 6 month) as well as at 3, 6 and 12 months postoperatively (3D-Shape, Erlangen, Germany) and in 15 healthy childs at the same age. The measure point density was 200 µm on the z-scale, measure time was 640 ms. Data triangulation and fusion was realized using specialized software (Slim3D, 3D-Shape, Erlangen, Germany) resulting in a 3D polygon grid. All data were converted into STL-format and copied into cephalometry software (Onyx Ceph, Image Instruments, Chemnitz, Germany). Each 3D cephalometric surface scan is analyzed according to the anthropometry standards. | — |
Countries
Germany
Contacts
Public ContactMarkus Martini
Klinik und Poliklinik für Mund-, Kiefer - und Plastische Gesichtschirurgie
Outcome results
None listed