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Fibrous Band between Extraocular Muscles in Unilateral Coronal Synostosis

Chung SA, Ha SJ

No abstract available.
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From Resection to Disconnection for Seizure Control in Pediatric Epilepsy Children

Hwang JK, Kim DS

Epilepsy surgery revealed dramatically improved seizure outcomes over medical therapy in drug-resistant epilepsy patients. Children with epilepsy, however, have multiple epileptic focuses which require multilobar resection for better seizure outcome....
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Baller-Gerold Syndrome in a Premature Infant with a Mutation in the RECQL4 Gene

Kim JS

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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Severe Hyperhidrosis in Apert Syndrome: A Case Report

Lee H, Choi S, Yang JH, Moon J, Suh DH

  • KMID: 2465921
  • Korean J Dermatol.
  • 2019 Nov;57(9):548-550.
Apert syndrome is a rare genetic disorder characterized by malformations of the skull, face, hands, and feet. We report a case of severe hyperhidrosis in a 13-month-old female infant with...
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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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Volumetric lipoinjection of the fronto-orbital and temporal complex with adipose stem cells for the aesthetic restoration of sequelae of craniosynostosis

Castro-Govea Y, Vela-Martinez A, Treviño-Garcia LA

BACKGROUND: Non-syndromic craniosynostosis causes craniofacial asymmetry and may persist after cranioplasty. These postoperative asymmetries are primarily depressions. In some cases, patients may be subjected to pranks and harassment by their...
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Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene

Cho WK, Ahn MB, Jang W, Chae H, Kim M, Suh BK

Most cases of congenital hyperthyroidism are autoimmune forms caused by maternal thyroid stimulating antibodies. Nonautoimmune forms of congenital hyperthyroidism caused by activating mutations of the thyrotropin receptor (TSHR) gene are...
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Neuroendoscopy: Current and Future Perspectives

Shim KW, Park EK, Kim DS, Choi JU

Neuroendoscopic surgery is performed because it causes minimal damage to normal structures, carries a lower rate of complications, and achieves excellent outcomes. Surgeons using an endoscope and related instruments can...
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A Case of Partial Short Arm Deletion in Chromosome 9 with Inguinal Hernia, Testicular Cystic Lesion, and Arthrogryposis Multiplex Congenita

Kim EJ, Chung SH, Park TS, Choi YS

Chromosome 9p syndrome is a rare chromosomal abnormality caused by a partial deletion in chromosome 9. It was first described in 1973 by Alfi et al., and has since been...
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The Unnecessity of Positron Emission Tomography Computed Tomography in the Etiologic Evaluation of Neurodevelopmental Delay in Craniosynostosis Patients

Yang CE, Park EK, Lee MC, Shim KW, Kim YO

BACKGROUND: In evaluation of craniosynostosis patients in terms of neurodevelopmental delay, positron emission tomography computed tomography (PET-CT) scan can be used to assess brain abnormalities through glucose metabolism. We aimed...
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Aesthetic Correction of Severe Facial Asymmetry in a Deformational Plagiocephaly Patient: A Case Report and Literature Review

Park JY, Kim HJ, Lee S, Jung SG

Deformational plagiocephaly (DP) (also referred to as positional plagiocephaly) has long posed challenges for plastic surgeons because it is difficult to differentiate from several other diseases, such as unilateral coronal...
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Two cases of Antley-Bixler syndrome caused by mutations in different genes, FGFR2 and POR

Woo H, Ko JM, Shin CH, Yang SW

Antley-Bixler syndrome (ABS) is a rare form of syndromic craniosynostosis with additional systemic synostosis, including radiohumeral or radioulnar synostosis. Another characteristic feature of ABS is mid-facial hypoplasia that leads to...
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Current and Future Perspectives in Craniosynostosis

Kang SG, Kang JK

Craniosynostosis has a varied clinical spectrum, ranging from isolated single suture involvement to multi-sutural fusions. Greater understanding of the pathogenesis of craniosynostosis has led to the development of practical treatment...
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Neurodevelopmental Problems in Non-Syndromic Craniosynostosis

Shim KW, Park EK, Kim JS, Kim YO, Kim DS

Craniosynostosis is the premature fusion of calvarial sutures, resulting in deformed craniofacial appearance. Hence, for a long time, it has been considered an aesthetic disorder. Fused sutures restrict growth adjacent...
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Distraction Osteogenesis Update: Introduction of Multidirectional Cranial Distraction Osteogenesis

Gomi A, Sunaga A, Kamochi H, Oguma H, Sugawara Y

In this review, we discuss in detail our current procedure for treating craniosynostosis using multidirectional cranial distraction osteogenesis (MCDO). The MCDO method allows all phenotypes of skull deformity to be...
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Minimally Invasive Suturectomy and Postoperative Helmet Therapy : Advantages and Limitations

Chong S, Wang KC, Phi JH, Lee JY, Kim SK

Various operative techniques are available for the treatment of craniosynostosis. The patient's age at presentation is one of the most important factors in the determination of the surgical modality. Minimally...
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Craniosynostosis : Updates in Radiologic Diagnosis

Kim HJ, Roh HG, Lee IW

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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Update of Diagnostic Evaluation of Craniosynostosis with a Focus on Pediatric Systematic Evaluation and Genetic Studies

Hwang SK, Park KS, Park SH, Hwang SK

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...
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Physiological Changes and Clinical Implications of Syndromic Craniosynostosis

Sakamoto H, Matsusaka , Kunihiro N, Imai K

Syndromic craniosynostosis has severe cranial stenosis and deformity, combined with hypoplastic maxillary bone and other developmental skeletal lesions. Among these various lesions, upper air way obstruction by hypoplastic maxillary bone...
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Craniosynostosis in Growing Children : Pathophysiological Changes and Neurosurgical Problems

Choi JW, Lim SY, Shin HJ

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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