- 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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- Craniometaphyseal Dysplasia
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Kim SR, Han YS
- KMID: 2167960
- Arch Plast Surg.
- 2013 Mar;40(2):157-159.
- doi: 10.5999/aps.2013.40.2.157
No abstract available. -
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- Half-and-Half Palatoplasty
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Han HH, Kang IS, Rhie JW
- KMID: 2134171
- Arch Craniofac Surg.
- 2014 Aug;15(2):105-108.
- doi: 10.7181/acfs.2014.15.2.105
A 14-month-old child was diagnosed with a Veau Class II cleft palate. Von Langenbeck palatoplasty was performed for the right palate, and V-Y pushback palatoplasty was performed for the left... -
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- Oblique transnasal wiring canthopexy via Y-V epicanthoplasty for telecanthus correction in a patient with Waardenburg syndrome
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Choi BG, Kim YH
- KMID: 2462489
- Arch Craniofac Surg.
- 2019 Oct;20(5):329-331.
- doi: 10.7181/acfs.2019.00395
Telecanthus is a common symptom accompanied by Waardenburg syndrome, a rare genetic disorder. The optimal surgery for telecanthus correction is still debated. A 28-year-old patient with Waardenburg syndrome underwent transnasal... -
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- Dear Members of the Association
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Yoon KC
- KMID: 2405040
- Arch Craniofac Surg.
- 2017 Dec;18(4):296-296.
- doi: 10.7181/acfs.2017.18.4.296
No abstract available. -
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- Anesthetic management of a child with Apert syndrome : A case report
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Kim YU, Choeong YS, Lee HM, Choi DK, Song JG, Choi KT
- KMID: 2046042
- Anesth Pain Med.
- 2009 Oct;4(4):352-354.
Apert syndrome involves abnormal growth of several bones such as craniofacial abnormalities, craniosynostosis and syndactyly of the feet and hands. Apert syndrome often demonstrates to the operating room for craniofacial... -
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- Hemifacial Spasm: A Neurosurgical Perspective
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Kong DS, Park K
- KMID: 1956209
- J Korean Neurosurg Soc.
- 2007 Nov;42(5):355-362.
- doi: 10.3340/jkns.2007.42.5.355
Hemifacial spasm (HFS) is characterized by tonic clonic contractions of the muscles innervated by the ipsilateral facial nerve. Compression of the facial nerve by an ectatic vessel is widely recognized... -
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- Ectopic Preauricular Sinus in a Facial Cleft and Microtia Patient
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Park JY, Lee S, Kim HJ, Jung SG
- KMID: 2405038
- Arch Craniofac Surg.
- 2017 Dec;18(4):287-291.
- doi: 10.7181/acfs.2017.18.4.287
Preauricular sinus is a congenital malformation that is very commonly encountered among the general population and it has especially high prevalence among Asians when compared to other ethnic groups. It... -
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- Clinical Application of Three-Dimensional Printing Technology in Craniofacial Plastic Surgery
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Choi JW, Kim N
- KMID: 1908398
- Arch Plast Surg.
- 2015 May;42(3):267-277.
- doi: 10.5999/aps.2015.42.3.267
Three-dimensional (3D) printing has been particularly widely adopted in medical fields. Application of the 3D printing technique has even been extended to bio-cell printing for 3D tissue/organ development, the creation... -
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- A Case of Branchio-oculo-facial Syndrome
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Park MY, Kim YC
- KMID: 2266293
- Ann Dermatol.
- 2009 Aug;21(3):288-290.
- doi: 10.5021/ad.2009.21.3.288
Branchio-oculo-facial syndrome (BOFS) is a rare, autosomal dominant disorder. It is characterized by distinct craniofacial abnormalities including abnormal location of the ears, aplastic cervical skin lesions, malformed auricles, conductive hearing... -
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- Pituitary Adenoma Accompanying Sphenoidal Meningoencephalocele with Clival Extension
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Kim TJ, Kim CH, Cheong JH, Kim JM
- KMID: 2189061
- J Korean Neurosurg Soc.
- 2005 Sep;38(3):242-244.
Encephaloceles are known as rare craniofacial developmental anomalies which are herniation of cranial contents through a skull defect. Sphenoidal meningoencephalocele represents an important cause of reVersible visual loss. We report... -
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- The 50 Most Cited Papers in Craniofacial Anomalies and Craniofacial Surgery
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Mahon NA, Joyce CW, Thomas S, Concannon , Murray D
- KMID: 2391870
- Arch Plast Surg.
- 2015 Sep;42(5):559-566.
- doi: 10.5999/aps.2015.42.5.559
BACKGROUND: Citation analysis is a recognized scientometric method of classifying cited articles according to the frequency of which they have been referenced. The total number of citations an article receives... -
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- A Case of Trisomy 9 Mosaicism Syndrome
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Na YJ, Lee JH, Park MS
- KMID: 2355576
- Perinatology.
- 2016 Sep;27(3):174-177.
- doi: 10.14734/PN.2016.27.3.174
Trisomy 9 mosaicism syndrome was first reported by Haslam in 1973 and has been rarely reported. The severity of malformations depends on the percentage of trisomic cells. This syndrome can... -
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- A Case of Partial Trisomy 9 due to Maternal Balanced Translocation t(9;21)(q21.2;q11.2)
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Shin IS, Jung WJ, Jin JY, Lee WR
- KMID: 1845273
- Korean J Perinatol.
- 2010 Sep;21(3):302-305.
Trisomy 9 syndrome was first reported by Retheore in 1970 and has been rarely reported. This syndrome consists of partial and complete trisomy 9. It is characterized by growth and... -
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- Craniofacial Asymmetry in Adults With Neglected Congenital Muscular Torticollis
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Jeong KY, Min KJ, Woo J, Yim SY
- KMID: 2165648
- Ann Rehabil Med.
- 2015 Jun;39(3):440-450.
- doi: 10.5535/arm.2015.39.3.440
OBJECTIVE: To evaluate the craniofacial asymmetry in adults with neglected congenital muscular torticollis (CMT) by quantitative assessment based on craniofacial three-dimensional computed tomography (3D-CT). METHODS: Preoperative craniofacial asymmetry was measured by... -
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- Soft tissue reconstruction in wide Tessier number 3 cleft using the straight-line advanced release technique
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Kim GH, Baek RM, Kim BK
- KMID: 2456818
- Arch Craniofac Surg.
- 2019 Aug;20(4):255-259.
- doi: 10.7181/acfs.2019.00276
Craniofacial cleft is a rare disease, and has multiple variations with a wide spectrum of severity. Among several classification systems of craniofacial clefts, the Tessier classification is the most widely... -
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- A case of Roberts syndrome
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Choi Y, Chung YH, Lim IS, Kim CH, Lee DK, Kim SN, Song SY, Chi JG
- KMID: 2042044
- J Korean Pediatr Soc.
- 1993 Oct;36(10):1447-1451.
Roberts syndrome is an autosomal recessive disorder accompanied by limb defects, craniofacial abnormalities, pre-and postnatal growth retardation. Patients with Roberts syndrome have characteristic premature separation of heterochromatin of many chromosomes... -
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- Ocular Findings in Cri Du Chat Syndrome: A Case Report
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Kim SK, Kim HS, Kim SH
- KMID: 2337749
- J Korean Ophthalmol Soc.
- 2008 Nov;49(11):1867-1870.
PURPOSE: To report the ophthalmologic examination of an infant who has cri du chat syndome with exotropia and facial abnormalities. CASE SUMMARY: A 7 - month - old infant was confirmed... -
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- A Case of Near Total Aortic Replacement in an Adolescent With Loeys-Dietz Syndrome
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Suh YJ, Kwon HW, Kim GB, Kwon BS, Bae EJ, Noh CI, Choi JY, Kim KH, Kim YJ, Park SS
- KMID: 2225025
- Korean Circ J.
- 2012 Apr;42(4):288-291.
- doi: 10.4070/kcj.2012.42.4.288
Loeys-Dietz syndrome is a recently described autosomal dominant disorder caused by mutations in the genes for transforming growth factor-beta receptor type 1 or 2 (TGF-ssR 1/2). The syndrome predisposes patients... -
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- A case of Larsen syndrome
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Kim JS, Kim SH, Kim JH, Jin CH, Kim HY, Song YR, Oh KY
- KMID: 2273531
- Korean J Obstet Gynecol.
- 2008 Nov;51(11):1337-1341.
Larsen syndrome is a rare congenital skeletal malformation (1 in 100,000 births) caused by a generalized mesenchymal connective tissue disorder. This disorder leads to a broad spectrum of anomalies. Major... -
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