- A Case of Craniofacial Dysostosis: Crouzon's Disease
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Oh CK, Moon HJ
- KMID: 2204630
- J Korean Ophthalmol Soc.
- 1976 Dec;17(4):567-571.
A monstrous faced, 60 years old famale patient was first seen in our clinic on May 1, 1976, complaining of diffuse abdominal pain. Throughout physical examination and x-ray study revealed... -
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- Three Cases of Familial Occurrence of Crouzon's Disease (Cranlofaeial Dysostosis)
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Oh KS, Han KS
- KMID: 2122602
- J Korean Ophthalmol Soc.
- 1980 Dec;21(4):651-656.
Craniofacial dysostosis, a well defined. rare syndrome first described by Crouzon in 1912, characteristically shows frontal bosses, prognathism, exophthalmos, exotropia, optic nerveatrophy and maxillary hypoplasia. Three cases of familial occurrence... -
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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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- Surgical Treatment of the Craniofacial Dysostoses-Crouzon's Disease
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Kang JK, Song JU, Kim JC, Lim P
- KMID: 2068317
- J Korean Neurosurg Soc.
- 1987 Mar;16(1):289-296.
Craniofacial dysostoses(Crouzon's disease) are characterized by cranial and facial deformities but the relationship between the craniosynostosis and facial deformities has not been clearly established. However, we believe that certain facial... -
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- Modification of Le Fort III Osteotomy and Fronto-orbital Advancement for the Correction of Crouzon's Disease
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Lee JS, Lee JG, Kim CS, Ha JW
- KMID: 2329684
- J Korean Cleft Palate-Craniofac Assoc.
- 2000 Oct;1(1):109-114.
In 1912, Crouzon reported one of craniofacial dysostosis, which was inherited as an autosomal dominant trait and characterized by craniosynostosis, midface hypoplasia, and exorbitism. In 1950, the first midface advancement... -
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- Clinical Experience for the Surgery in the Craniofacial Dysostosis: Reports of Nine Operative Cases
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Kang JK, Song JU
- KMID: 2068299
- J Korean Neurosurg Soc.
- 1987 Mar;16(1):103-116.
The craniofacial dysostoses are due to synostosis of the basal skull sutures in the anterior cranial fossa. Patients with these abnormalities potentially have normal brains that are distorted by the... -
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- COMBINED SURGICAL METHODS FOR CORRECTION OF CROUZON'S DISEASE IN ADULTS: MODIFIED FRONTOFACIAL MONOBLOC ADVANCEMENT AND CRANIAL VAULT REMODELING
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Lee YH, Mun GH
- KMID: 1921397
- J Korean Soc Plast Reconstr Surg.
- 1997 Nov;24(6):1295-1303.
No abstract available. -
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- A Case of Crouzon's Disease
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Cha D, Ahn H
- KMID: 2127626
- J Korean Ophthalmol Soc.
- 1991 Aug;32(8):694-697.
Crouzon's disease is a peculiar type of craniosynostosis which is premature closure of the suture, and deformities of craniofacial bone. Such a many deformities are caused by continuing brain growth... -
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- How to Make the Blockage between the Nasal Cavity and Intracranial Space in Craniofacial Surgery
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Lee Y, Kim WJ
- KMID: 2203689
- J Korean Soc Plast Reconstr Surg.
- 2002 May;29(3):136-140.
Craniofacial surgery for facial advancement or correction of severe craniofacial malformations such as orbital hypertelorism, Crouzon's disease and Apert's syndrome may bring about great risk. Especially postoperative infection in the... -
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- Midfacial distraction osteogenesis of Crouzon syndrome with RED(Rigid External Distraction) system
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Lee YK, Choi JH, Kim SH, Baek SH, Chang YI
- KMID: 1610021
- Korean J Orthod.
- 2002 Jun;32(3):175-183.
Crouzon syndrome is one of the craniofacial syndromes characterized by craniosynostosis, midfacial hypolpasia and ocular proptosis. Distraction osteogenesis is becoming important technique to treat craniofacial dysplaisa. It has many advantages... -
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- Cranioplasty with Absorbable Plates for Craniosynostosis
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Park SW, Kang DH, Yoon ES, Koo SH, Park SH
- KMID: 1961963
- J Korean Cleft Palate-Craniofac Assoc.
- 2001 Oct;2(2):97-102.
With the introduction of smaller metallic plating systems, many surgeons have adopted their use for craniofacial procedures in infants and small children. However, this metallic plating system had problems associated... -
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- A Case of Crouzon's Disease
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Rhee CW, Kim HC
- KMID: 1659476
- J Korean Ophthalmol Soc.
- 1977 Jun;18(2):227-229.
Normally the cranial bones are closed finally in early adulthood; thus, premature closure of one or more sutures of the skull results in a head deformity producing damaging effects to... -
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- Multidrug-Resistant Streptococcus pneumoniae Sepsis and Meningitis after Craniofacial Surgery: Case Report
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Kim H, Lim SY, Pyon JK, Mun GH, Bang SI, Oh KS
- KMID: 2322460
- J Korean Soc Plast Reconstr Surg.
- 2011 Jul;38(4):516-518.
PURPOSE: The prevalence of antibiotic-resistant Streptococcus pneumoniae meningitis has increased worldwide. There are some reports about postoperative antibiotic-resistant Streptococcus pneumoniae infection after craniofacial surgery, but, there is no report in... -
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- Extensive Subperiosteal Craniectomy of Crouzon's Disease
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Park YG, Lee KC, Choi JU, Kim YS, Chung SS, Lee HJ
- KMID: 2187186
- J Korean Neurosurg Soc.
- 1979 Sep;8(2):577-582.
The authors present a case of Crouzon's disease with advanced craniostenosis and exophthalmos. Extensive subperiosteal resection of the vault and base of the skull resulted obvious decompression of the brain... -
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- Monoblock Craniofacial Internal Distraction in a Child with Pfeiffer Syndrome: A Case Report
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Chung J, Park DH, Yoon SH
- KMID: 1713473
- J Korean Med Sci.
- 2008 Apr;23(2):342-346.
- doi: 10.3346/jkms.2008.23.2.342
A 7-yr-old boy visited our surgical center with Pfeiffer syndrome type 1, presenting with macrocrania, broad big toe and thumb, exophthalmos, tongue protrusion, malocclusion with midfacial retrusion, mild respiratory difficulty... -
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- Craniofacial morphologic alteration induced by bone-targeted mutants of FGFR2 causing Apert and Crouzon syndrome
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Lee KJ, Nah HD, Tjoa ST, Park YC, Baik HS, Yun TM, Song JW
- KMID: 2273587
- Korean J Orthod.
- 2006 Aug;36(4):284-294.
OBJECTIVE: Activating mutations in the fibroblast growth factor receptor-2 (FGFR2) have been shown to cause syndromic craniosynostosis such as Apert and Crouzon syndromes. The purpose of this pilot study was... -
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- Le Fort III Advancement for the Correction of Crouzon's Disease
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Park CG, Park SJ
- KMID: 2119552
- J Korean Soc Plast Reconstr Surg.
- 1999 Jul;26(4):590-596.
Crouzon's disease, first described by Crouzon in 1912, is characterized by craniosynostosis, exorbitism and midface hypoplasia. As well, it has been known to be transmitted as an autosomal dominant trait.... -
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- A Case of Crouzon's Disease
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Sohn MS, Kim WS, Oh SK, Kang SK, Kim CN, Lee IH
- KMID: 2107010
- J Korean Ophthalmol Soc.
- 1970 Dec;11(4):83-86.
A case of Crouzon's disease, in spite of the relatively small number of cases reported until recently. The patient was 3years old male and hospitalized Woo-Sok University hospital 5 May,... -
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- A Case of FGFR2 Exon lllc Mutation in Crouzon Syndrome
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Bae SC, Lee EH, Park MS, Hahn SH, Hong CH
- KMID: 2104438
- J Korean Pediatr Soc.
- 1998 Dec;41(12):1717-1721.
Crouzon syndrome, an autosomal dominant disorder, has characteristic features of craniosynostosis, hypertelorism, exophthalmos, maxillary hypoplasia and relative mandibular prognathism. Mutations of fibroblast growth factor receptor 2 (FGFR2) gene are associated... -
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- Midface Advancement with Rigid External Distraction System in Crouzon's Disease
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Kim SW, Park JK, Park CG, Baek SH, Choi JH
- KMID: 2119857
- J Korean Soc Plast Reconstr Surg.
- 2003 Sep;30(5):532-540.
Distraction osteogenesis has become an alternative technique to treat craniomaxillofacial anomalies. It was initially used to treat mandibular dysplasia and now it is applied to other regions of the craniofacial... -
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