1.Preoperative Planning for Reconstruction of Apert Skull.
Young Soo KIM ; Hee Yeun CHOI ; Sun Il KIM
Journal of Korean Neurosurgical Society 1997;26(12):1733-1738
Apert syndrome is characterized by a hyperacrobrachycephalic skull with a flattened occiput, and malformations of the midface, hands and feet, as well as complicated multiple craniosynostosis and dysmorphism of the skull. Several authors have recently reported in the treatment of complicated skull anomalies that simple x-ray and axial/coronal CT imaging cannot provide sufficiently precise information, and presurgical planning cannot be based on the findings of these procedures ; three-dimensional(3D) reconstruction of CT images is, instead, needed. By means of a computerized simulation, the authors reformatted skull contour on a monitor using the method of splitting and remodeling a 3D skull image. Surgery was performed and the result was good. Presurgical computerized simulation was thus shown to be very helpful for the surgical correction of complicated craniosynostosis.
Acrocephalosyndactylia
;
Craniosynostoses
;
Foot
;
Hand
;
Skull*
2.Preoperative Planning for Reconstruction of Apert Skull.
Young Soo KIM ; Hee Yeun CHOI ; Sun Il KIM
Journal of Korean Neurosurgical Society 1997;26(12):1733-1738
Apert syndrome is characterized by a hyperacrobrachycephalic skull with a flattened occiput, and malformations of the midface, hands and feet, as well as complicated multiple craniosynostosis and dysmorphism of the skull. Several authors have recently reported in the treatment of complicated skull anomalies that simple x-ray and axial/coronal CT imaging cannot provide sufficiently precise information, and presurgical planning cannot be based on the findings of these procedures ; three-dimensional(3D) reconstruction of CT images is, instead, needed. By means of a computerized simulation, the authors reformatted skull contour on a monitor using the method of splitting and remodeling a 3D skull image. Surgery was performed and the result was good. Presurgical computerized simulation was thus shown to be very helpful for the surgical correction of complicated craniosynostosis.
Acrocephalosyndactylia
;
Craniosynostoses
;
Foot
;
Hand
;
Skull*
3.Clinical experience of craniosynostosis.
Son Ho PARK ; Jung Youn LEE ; Hee Chang AHN ; Yea Sik HAN
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1992;19(5):791-800
No abstract available.
Craniosynostoses*
4.A surgical correction of the isolated craniosynostosis.
Eul Je CHO ; Byung Yoon PARK ; Young Ho LEE ; Joong Uhn CHOI
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1992;19(5):761-771
No abstract available.
Craniosynostoses*
5.Surgical treatment of acrocephaly: a case report.
In Kwon CHOI ; Suk Wha KIM ; Jin Whan KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(4):838-843
No abstract available.
Craniosynostoses*
6.Preface : Invited Issue Editor, Professor Joon-Ki Kang, and the Topic, Craniosynostosis.
Journal of Korean Neurosurgical Society 2016;59(3):185-186
No abstract available.
Craniosynostoses*
7.A review of craniofacial syndromes.
Acta Medica Philippina 2017;51(3):162-166
Craniosynostoses are a complex and heterogenous group of conditions. The purpose of this review is to describe the entity of craniosynostosis and its associated genes along with the opthalmic ans systemic findings. Several genes such as FGRs,TWIST1, and MSX2 are involved in both syndromic and non-syndromic craniosynostosis.
Craniosynostoses
8.Apert Syndrome: A Report of One Case
Jun Kyoung HWANG ; Dong Sik LEE ; Jung Kun LIM ; Jong Sool SONG
The Journal of the Korean Orthopaedic Association 1986;21(5):939-942
Apert described acrocephalosyndactly as a clinical entity in 1906. The classic description of this syndrome includes patient with a combination of acrocephaly and syndactyly of either fingers, toes or both. More than 200 cases have been reported in the world literature. Authors experienced on case of the classic pattern of Apert syndrome and treated surgically for syndactyly. This one case was reported on this paper with brief review of the relevant literatures.
Acrocephalosyndactylia
;
Craniosynostoses
;
Fingers
;
Humans
;
Syndactyly
;
Toes
9.Apert Syndrome A Case Report and Analysis of the Reported Cases in Korea
Myung Sik PARK ; Tae Hoon CHOI
The Journal of the Korean Orthopaedic Association 1988;23(3):904-910
Apert syndrome, or acrocephalosyndactyly is a complex of associated malformations, which are craniosynostosis and symmetric complex syndactyly of the hands and feet. The syndrome was first described by Apert in 1906. Review of the worlds literature disclosed about 200 similar cases and 9 Cases in Korea. Authors experienced one case of Apert syndrome and treated surgically for acro-syndactyly and polydactyly of both hands and feet. The case was compared with the other previously reported cases in Korea.
Acrocephalosyndactylia
;
Craniosynostoses
;
Foot
;
Hand
;
Korea
;
Polydactyly
;
Syndactyly
10.Fibrous Band between Extraocular Muscles in Unilateral Coronal Synostosis
Korean Journal of Ophthalmology 2020;34(1):88-89
No abstract available.
Craniosynostoses
;
Muscles