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Oblique transnasal wiring canthopexy via Y-V epicanthoplasty for telecanthus correction in a patient with Waardenburg syndrome

Choi BG, Kim YH

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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Soft tissue reconstruction in wide Tessier number 3 cleft using the straight-line advanced release technique

Kim GH, Baek RM, Kim BK

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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Prenatal ultrasonography of craniofacial abnormalities

Mak AS, Leung KY

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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Dear Members of the Association

Yoon KC

No abstract available.
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Ectopic Preauricular Sinus in a Facial Cleft and Microtia Patient

Park JY, Lee S, Kim HJ, Jung SG

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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Mucoperiosteal Flap Necrosis after Primary Palatoplasty in Patients with Cleft Palate

Rossell-Perry P, Cotrina-Rabanal O, Barrenechea-Tarazona L, Vargas-Chanduvi R, Paredes-Aponte L, Romero-Narvaez C

BACKGROUND: The prevalence of flap necrosis after palatoplasty in patients with cleft palate. The prevalence of mucoperiosteal flap necrosis after palatoplasty remains unknown, and this complication is rare. This event...
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Upper airway and obstructive sleep apnea in children

Jee HM

Obstructive sleep apnea (OSA) is characterized by a disorder of breathing with prolonged partial and/or complete airway obstruction which causes frequent arousal during sleep. The prevalence of OSAS is approximately...
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A Case of Trisomy 9 Mosaicism Syndrome

Na YJ, Lee JH, Park MS

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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The Importance of Multidisciplinary Management during Prenatal Care for Cleft Lip and Palate

Han HH, Choi EJ, Kim JM, Shin JC, Rhie JW

BACKGROUND: The prenatal ultrasound detection of cleft lip with or without cleft palate (CL/P) and its continuous management in the prenatal, perinatal, and postnatal periods using a multidisciplinary team approach...
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The 50 Most Cited Papers in Craniofacial Anomalies and Craniofacial Surgery

Mahon NA, Joyce CW, Thomas S, Concannon , Murray D

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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Craniofacial Asymmetry in Adults With Neglected Congenital Muscular Torticollis

Jeong KY, Min KJ, Woo J, Yim SY

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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Clinical Application of Three-Dimensional Printing Technology in Craniofacial Plastic Surgery

Choi JW, Kim N

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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The First Korean Patient with Potocki-Shaffer Syndrome: A Rare Cause of Multiple Exostoses

Sohn YB, Yim SY, Cho EH, Kim OH

Potocki-Shaffer syndrome (PSS, OMIM #601224) is a rare contiguous gene deletion syndrome caused by haploinsufficiency of genes located on the 11p11.2p12. Affected individuals have a number of characteristic features including...
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A New Ultrasound Method for Assessment of Head Shape Change in Infants With Plagiocephaly

Kim JK, Kwon DR, Park GY

OBJECTIVE: To compare a new ultrasound measurement method with calliper cephalometry in infants with deformational plagiocephaly (DP) and to assess the differences of two methods according to the severity of...
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Half-and-Half Palatoplasty

Han HH, Kang IS, Rhie JW

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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Obstructive Sleep Apnea Syndrome in Children

Oh JI, Lee SH

Obstructive sleep apnea is characterized by partial or complete upper airway obstruction which leads to reduction of blood oxygenation often accompanied by frequent arousal during sleep. Obstructive sleep apnea in...
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An Unusual Presentation of Diabetic Ketoacidosis in Familial Hajdu-Cheney Syndrome: A Case Report

Lee GH, An SY, Sohn YB, Jeong SY, Chung YS

A 21-year-old man with diabetic ketoacidosis (DKA) displayed short and clubbed fingers and marked eyebrow, which are typical of Hajdu-Cheney Syndrome (HCS). Laboratory findings confirmed type 1 diabetes mellitus (DM)....
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A unique case of Turner syndrome accompanying prolactinoma and unexpected elongated styloid process: Clinical and cone-beam computed tomographic features

Evlice B, Tatli U, Yazicioglu I, Evlice A, Oztunc H

Turner syndrome (TS) is one of the most common chromosomal abnormalities, with an estimated frequency among female live births of 1/2,000-3,000. The syndrome is characterized by the partial or complete...
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Pyriform Sinus Fistula: A Single Center Experience

Seok JH, Ahn D, Sohn JH, Choi JH, Jung YY, Kong JS

BACKGROUND AND OBJECTIVES: Pyriform sinus fistula with 3rd and 4th branchial cleft anomaly is an extremely rare congenital condition that is not very well understood owing to its rarity. The...
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Craniometaphyseal Dysplasia

Kim SR, Han YS

No abstract available.
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