- In vitro Fusion of the Posterior Frontal Calvarial Suture in the Mouse
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Roh TS, Rah DK, Park C, Park BY
- KMID: 2041068
- J Korean Soc Plast Reconstr Surg.
- 2000 Nov;27(6):670-674.
The mechanism underlying cranial suture fusion remains yet unknown. An in vitro tissue culture model of cranial sutures permits exclusion of biomechanical factors that may affect the fusion and patency... -
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- Development and Growth of the Normal Cranial Vault : An Embryologic Review
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Jin SW, Sim KB, Kim SD
- KMID: 2192084
- J Korean Neurosurg Soc.
- 2016 May;59(3):192-196.
- doi: 10.3340/jkns.2016.59.3.192
Understanding the development of a skull deformity requires an understanding of the normal morphogenesis of the cranium. Craniosynostosis is the premature, pathologic ossification of one or more cranial sutures leading... -
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- Quantitative Analysis of Developmental Process of Cranial Suture in Korean Infants
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Sim SY, Yoon SH, Kim SY
- KMID: 2190465
- J Korean Neurosurg Soc.
- 2012 Jan;51(1):31-36.
- doi: 10.3340/jkns.2012.51.1.31
OBJECTIVE: The purpose of this study was to elucidate the anatomical development of physiologic suture closure processes in infants using three dimensional reconstructed computed tomography (CT). METHODS: A consecutive series of... -
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- Two cases of craniofacial dysostosis
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Yu SK, Kang KH, Koh KJ
- KMID: 1515652
- Korean J Oral Maxillofac Radiol.
- 2004 Sep;34(3):165-169.
Craniofacial dysostosis is considered to be one of rarely observed syndromes characterized by premature closing of all cranial sutures. The first patient was a 4-year-old male infant who had been... -
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- Mercedes Benz Pattern Craniosynostosis: A Case Report
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Ryoo S, Lim SY, Mun GH
- KMID: 2220363
- J Korean Soc Plast Reconstr Surg.
- 2011 Sep;38(5):683-686.
PURPOSE: Craniosynostosis of three or more cranial sutures was not common. "Mercedes Benz pattern," named by Moore1 was a rare form of craniosynostosis and had an atypical pattern of premature... -
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- A Case of Late Onset Atypical Craniosynostosis
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Kim KR, Seok LJ, Lee JS
- KMID: 2329436
- J Korean Child Neurol Soc.
- 2009 Nov;17(2):242-246.
Craniosynostosis is a congenital deformity causing disorder in the growth of the skull and brain parenchyma, resulting from the fusion of the cranial sutures of calvaria or basilar before birth... -
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- Baller-Gerold Syndrome in a Premature Infant with a Mutation in the RECQL4 Gene
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Kim JS
- KMID: 2466646
- Neonatal Med.
- 2019 Nov;26(4):240-245.
- doi: 10.5385/nm.2019.26.4.240
Baller-Gerold syndrome is a rare autosomal recessive disorder characterized by premature fusion of the cranial sutures and malformation of the upper limb extremities at birth. Although the pathogenesis of Baller-Gerold... -
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- Genetic Syndromes Associated with Craniosynostosis
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Ko JM
- KMID: 2192082
- J Korean Neurosurg Soc.
- 2016 May;59(3):187-191.
- doi: 10.3340/jkns.2016.59.3.187
Craniosynostosis is defined as the premature fusion of one or more of the cranial sutures. It leads not only to secondary distortion of skull shape but to various complications including... -
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- Effectiveness of Helmet Cranial Remodeling in Older Infants with Positional Plagiocephaly
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Kim HY, Chung YK, Kim YO
- KMID: 2134160
- Arch Craniofac Surg.
- 2014 Aug;15(2):47-52.
- doi: 10.7181/acfs.2014.15.2.47
BACKGROUND: Management of positional plagiocephaly by wearing a cranial molding helmet has become a matter of growing medical interest. Some research studies reported that starting helmet therapy early (age 5... -
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- Craniosynostosis in Growing Children : Pathophysiological Changes and Neurosurgical Problems
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Choi JW, Lim SY, Shin HJ
- KMID: 2192086
- J Korean Neurosurg Soc.
- 2016 May;59(3):197-203.
- doi: 10.3340/jkns.2016.59.3.197
Craniosynostosis is defined as the premature fusion of one or more cranial sutures resulting in skull deformity. Characteristically, this disorder can cause diverse neurosurgical problems, as well as abnormal skull... -
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- Generation of a transgenic mouse model to study cranial suture development; Apert syndrome
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Lee KJ, Ratisoontorn C, Baik HS, Park YC, Park KK, Nah HD
- KMID: 1976478
- Korean J Orthod.
- 2003 Dec;33(6):485-497.
The form and function of the craniofacial structure critically depend on genetic information. With recent advances in the molecular technology, genes that are important for normal growth and morphogenesis of... -
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- A Case of Apert's Syndrome with Encephalocele and Hypogenesis of Corpus Callosum
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Kwon MK, Yun JY, Kim MR, Lee KH, Lee HR, Kim KN
- KMID: 1946213
- J Korean Pediatr Soc.
- 2001 Jul;44(7):832-836.
Apert's syndrome(acrocephalosyndactyly) is a rare congenital anomaly that is characterized by the combination of premature fusion of multiple cranial sutures primarily involving the coronal suture and severe symmetrical syndactyly of... -
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- The Supplementary Use of BoneSource(R) in the Surgical Correction of Craniosynostosis
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Lim JH, Song JK, Yoo G, Byeon JH
- KMID: 2203408
- J Korean Soc Plast Reconstr Surg.
- 2005 Jul;32(4):474-478.
Craniosynostosis is a congenital anomaly characterized by premature closure of cranial sutures. Surgical intervention should be performed during infancy. However, surgical correction of craniosynostosis remains bone defect and secondary angle... -
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- Craniosynostosis : Updates in Radiologic Diagnosis
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Kim HJ, Roh HG, Lee IW
- KMID: 2192091
- J Korean Neurosurg Soc.
- 2016 May;59(3):219-226.
- doi: 10.3340/jkns.2016.59.3.219
The purpose of this article is to review imaging findings and to discuss the optimal imaging methods for craniosynostosis. The discussion of imaging findings are focused on ultrasonography, plain radiography,... -
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- Cleidocranial dysplasia: a case report
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Han JW
- KMID: 1573819
- Korean J Oral Maxillofac Radiol.
- 2005 Dec;35(4):225-229.
Cleidocranial dysplasia is a rare, autosomal dominant congenital disorder. A 12-year old female visited with chief complaint of unerupted permanent teeth. Also her father showed severe class III malocclusion. The... -
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- Transient Bulging of the Fontanelle in Infants after a Febrile Illness without Central Nervous System Infection
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Bae SH, Kim YO, Kim SJ, Son YJ, Woo YJ
- KMID: 1730009
- Chonnam Med J.
- 2010 Aug;46(2):117-120.
- doi: 10.4068/cmj.2010.46.2.117
Increased intracranial pressure in infants with open cranial sutures can cause bulging of the anterior fontanelle. This condition is referred to as transient bulging of the fontanelle (TBF) if the... -
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- Prenatal ultrasonography of craniofacial abnormalities
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Mak AS, Leung KY
- KMID: 2433288
- Ultrasonography.
- 2019 Jan;38(1):13-24.
- doi: 10.14366/usg.18031
Craniofacial abnormalities are common. It is important to examine the fetal face and skull Epub ahead of print during prenatal ultrasound examinations because abnormalities of these structures may indicate the... -
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- Craniosynostosis Occurring between Siblings
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Choi JH, Kim MH, Kim MS, Jung GY, Lee KC, Kim SK
- KMID: 2266979
- Arch Craniofac Surg.
- 2013 Oct;14(2):115-118.
- doi: 10.7181/acfs.2013.14.2.115
Craniosynostosis is a congenital anomaly in which cranial sutures close prematurely and restrict skull growth. In this paper, the case of two siblings, a male and a female, who were... -
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- Isotretinoin Treatment for the Recalcitrant Acne on a Patient with Apert Syndrome
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Byun J, Han S, Yang BH, Song HJ, Lee HS, Lee SG, Shin J, Choi GS
- KMID: 2301953
- Korean J Dermatol.
- 2009 Oct;47(10):1196-1198.
Apert syndrome is a rare genetic craniofacial disorder associated with premature fusion of multiple cranial sutures and syndactyly. It is caused by mutation in the fibroblast growth factor receptor 2... -
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- A case of restrictive dermopathy
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Lee SI, Hong CH, Cheong YH, Kang MS, Sin JB
- KMID: 2279253
- Korean J Pediatr.
- 2007 Mar;50(3):306-310.
- doi: 10.3345/kjp.2007.50.3.306
Restrictive dermopathy is a rare autosomal recessive disorder in which rigidity or tautness of the skin from the second trimester causes a fetal akinesia deformation sequence (FADS) and early death.... -
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