1.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*
2.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*
3.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*
4.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*
5.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
6.Fibrous Band between Extraocular Muscles in Unilateral Coronal Synostosis
Korean Journal of Ophthalmology 2020;34(1):88-89
No abstract available.
Craniosynostoses
;
Muscles
7.A Case of Scaphocephaly in a Newborn.
Journal of the Korean Pediatric Society 1985;28(3):297-300
No abstract available.
Craniosynostoses*
;
Humans
;
Infant, Newborn*
8.Update of Diagnostic Evaluation of Craniosynostosis with a Focus on Pediatric Systematic Evaluation and Genetic Studies.
Su Kyeong HWANG ; Ki Su PARK ; Seong Hyun PARK ; Sung Kyoo HWANG
Journal of Korean Neurosurgical Society 2016;59(3):214-218
Most craniosynostoses are sporadic, but may have an underlying genetic basis. Secondary and syndromic craniosynostosis accompanies various systemic diseases or associated anomalies. Early detection of an associated disease may facilitate the interdisciplinary management of patients and improve outcomes. For that reason, systematic evaluation of craniosynostosis is mandatory. The authors reviewed systematic evaluation of craniosynostosis with an emphasis on genetic analysis.
Craniosynostoses*
;
Diagnosis
;
Humans
9.Right Angled Z-osteotomy in Total Cranial Vault Remodeling in Sagittal Synostosis.
Journal of the Korean Society of Plastic and Reconstructive Surgeons 2002;29(4):348-351
Sagittal synostosis is the most common isolated craniosynostosis and usually recognized in early infancy. Numerous surgical techniques including strip craniectomy, the pi procedure, subtotal calvariectomy have been used, and they are usually successful if carried out in early infancy. Unfortunately, some children with sagittal synostosis are not considered for surgical correction by the age of 2 years. From March 2001 to February 2002, we have experienced two children older than 2 years of age with sagittal synostosis, and in all cases, performed total cranial vault remodeling with minimal bony defect. Reconstruction consisted of shortening of the sagittal midline strut, barrel stave osteotomy of temporal region, and right angled Z-osteotomy of parieto-occipital region. Using right angled Z-osteotomy, we can easily reshape and fix parieto-occipital bone flap with good stability and esthetic results. We report our technique for the late correction of scaphocephaly in two children with satisfactory results
Child
;
Craniosynostoses*
;
Humans
;
Osteotomy
10.Immediate Spontaneous Shape Correction Using Expantile Zigzag Craniectomy in Infantile Scaphocephaly: Is There an Improvement in the Developmental Quotient Following Surgery?.
Journal of Korean Neurosurgical Society 2011;49(3):194-199
There is still debate over which method of the surgery is the most appropriate for the treatment of scaphocephalic infants. In addition, change in psychomotor development following these procedures is a very complex issue that has not yet been resolved. In this paper, the authors describe a surgical technique for immediate spontaneous shape correction of infantile scaphocephaly. There were significant differences between pre- and postoperative cephalic index. We also describe an improvement in the developmental quotient following surgery. Therefore, this expantile zigzag craniectomy should be recommended to correct for isolated sagittal craniosynostosis in infants.
Craniosynostoses
;
Humans
;
Infant
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